China Stroke Primary Prevention Trial 2 for Participants with Hypertension and MTHFR 677 TT Genotype
- Conditions
- HypertensionMTHFR 677 TT GenotypeHypertensionMTHFR 677 TT Genotype
- Interventions
- Drug: 5-methyltetrahydrofolate (5-MTHF)Drug: 5-MTHF Placebos
- Registration Number
- NCT04974151
- Lead Sponsor
- Shenzhen Ausa Pharmed Co.,Ltd
- Brief Summary
This is a multi-center, randomized, double-blind, triple-dummy, controlled trial in 24,000 Chinese men and women with hypertension and MTHFR 677 TT genotype.
The study participants will be randomized to one of the three treatment groups:
Group A: amlodipine tablet (5mg), taken orally, once daily, serving as active comparator.
Group B: amlodipine folic acid 5.8mg tablet (5mg amlodipine and 0.8mg folic acid), taken orally, once daily.
Group C: amlodipine folic acid 5.8mg tablet plus 5-methyltetrahydrofolate (5-MTHF, 0.4mg), taken orally, once daily.
The primary endpoint is first ischemic stroke.
- Detailed Description
This study consists of 3 periods: Screening, Run-in, and Randomized treatment.
Period I: Screening (V0)
The purpose of Period I is to obtain informed consent and screen for eligible participants.
After obtaining written informed consent, at the screening visit (V0), participants will complete a face-to-face interview and clinical evaluation and measurements. Their biological samples will be collected for laboratory analyses. Collectively, these information will help to determine eligibility for inclusion in the study.
Period II: Run-in Period (VD)
The purpose of Run-in is to assess participants' compliance for following the amlodipine treatment regimen as well as to observe participants' tolerance to amlodipine, so as to screen out those with poor compliance or intolerance to amlodipine treatment.
The run-in phase lasted 2 to 4 weeks, during which oral administration of Amlodipine tablets (5 mg) was given once daily.
Period III: Randomized Treatment (V1-V21)
This is a 5-year period of randomized, double-blind, triple-dummy, controlled treatment. At each of the research centers, participants who remain eligible for participation in the study will be randomized into 3 treatment groups:
A. Amlodipine-only (5mg/d) with an amlodipine folic acid placebo and 5-MTHF placebos.
B. Amlodipine folic acid tablet (5.8mg/d) with amlodipine placebo and 5-MTHF placebo.
C. Amlodipine folic acid tablets (5.8mg/d) and 5-MTHF (0.4mg/d) with an amlodipine placebo in a 1:1:1 ratio, using the randomization and trial supply management (RTSM) platform.
During the treatment period, other antihypertensive drugs can be added to achieve blood pressure control (BP ≤140/90mmHg), including Valsartan (80mg/d), or/and Indapamide (1.5mg/d), or/and metoprolol tartrate tablets (25mg/d). Participants will be followed up every 3 months during the treatment period, and the treatment drugs will be distributed at each visit.
A total of 24,000 participants will be randomly assigned to one of three treatment groups (Group A n=8,000, Group B n=8,000, Group C n=8,000). Based on published data from CSPPT (Huo et al, JAMA, 2015), the 5-year cumulative incidence of first ischemic stroke in the amlodipine-only group is 3.5%. Assuming the 5-year cumulative incidence of first ischemic stroke in the amlodipine-only group is around 3.5%, this trial has 80% power to detect a 20% difference between group A and group B+C in the observed hazard ratio (HR) for incident ischemic stroke (HR≤0.80), at a two-sided significance level of α=0.05. If instead, the 5-year incidence of ischemic stroke in the amlodipine-only group is 2.5%, this trial has 80% power to detect a 23% difference between the treatment groups (A vs B+C) (HR≤0.77).
There are two planned interim analyses, one at the end of the third year, and another at the end of the fourth year. The O'Brien-Fleming alpha-spending function will be used to define the significance level of each interim analysis to ensure that the final overall two-sided significance level of α=0.05 is met.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 24000
- Men and women, aged ≥45 and <75 years.
- Hypertension: Previously diagnosed with primary hypertension and has been taking antihypertensive medication within the past two weeks; OR has not been taking antihypertensive medications within the last two weeks, but meets the following criteria for hypertension: SBP≥140 mmHg and/or DBP≥90 mmHg (average of at least 2 measurements each time) at two separate (not on the same day) clinical visits.
- MTHFR 677 TT genotype (based on the test results from the central laboratory during the screening period or a previous official test report from a laboratory with medical testing qualifications).
- Voluntarily participates and has given signed informed consent.
Randomized-treatment phase inclusion criteria:
- Good compliance during the run-in period, and unlikely to discontinue treatment;
- No stroke or cardiovascular events during the run-in period;
- The participant voluntarily agrees to continue the study.
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Previously diagnosed secondary hypertension;
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Previously diagnosed stroke;
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Previously diagnosed myocardial infarction;
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Previously diagnosed heart failure;
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Previously diagnosed atrial fibrillation;
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Cardio-cerebral-kidney revascularization and/or other large arterial stent;
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Currently on dialysis, or diagnosed with stage 4-5 chronic kidney disease, or eGFR <30 mL/ min/1.73m²;
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Known to have congenital (such as aortic stenosis) or acquired organic heart disease;
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Known to have any of the following severe diseases or conditions:
- Digestive system: i. Previously diagnosed with any form of viral hepatitis that is currently still in the active phase; ii. Abnormal liver function test before enrollment (any of ALT, AST, GGT, TBIL, DBIL test 3 times higher than normal, or ALB≤30g/L); iii. Subtotal gastrectomy and/or gastrojejunostomy;
- Respiratory system: previously diagnosed with pulmonary heart disease;
- Presence of malignant tumors or other severe diseases;
- Presence of long-term gastrointestinal symptoms such as ; anorexia, decreased appetite, nausea, and abdominal bloating;
- Previously diagnosed with vitamin B12 deficiency and/or its related diseases.
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Participant, at the investigator's discretion, is assessed to be unsuitable for the study, for reasons including but not limited to the presence of abnormal laboratory results, or clinical conditions;
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Prior history of significant intolerance due to adverse reactions resulting from usage of amlodipine or other CCBs, valsartan or other ARBs, indapamide or other similar diuretics, metoprolol tartaric acid or other beta-blockers, or any drugs or health products containing folate or folic acid;
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Regular consumption of folic acid or vitamin B compounds, or other compounds containing folic acid in the past 3 months;
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The presence of any of the following conditions that could negatively influence a participant's ability to consent or participate in the trial:
- Dementia;
- Severe mental disorders;
- Inability to express informed consent;
- Unlikely to complete the study follow-up as specified by the protocol, or plans to relocate outside of the study area in the near future;
- History of poor compliance when taking antihypertensive medications or is expected to have poor compliance during the study;
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Refusal to participate, or inability to modify current drug regimen;
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Women who are pregnant or breastfeeding; or subjects of childbearing potential who are unwilling or unable to use effective contraception during the study period.
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Within one month prior to the first visit, having participated in any clinical trial for a drug that has not yet been officially approved by the state or is not currently approved for sale; or currently participating in any clinical trial that could potentially impact the results of this study (medication use, drug efficacy, drug interaction, etc.).
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Amlodipine (5mg/d) Amlodipine besylate Amlodipine 5mg x1 tablet + Amlodipine folic acid (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine tablets, amlodipine folic acid placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine 5mg x2 tablets + amlodipine folic acid (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine (5mg/d) Amlodipine folic acid placebo Amlodipine 5mg x1 tablet + Amlodipine folic acid (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine tablets, amlodipine folic acid placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine 5mg x2 tablets + amlodipine folic acid (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine (5mg/d) 5-MTHF Placebos Amlodipine 5mg x1 tablet + Amlodipine folic acid (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine tablets, amlodipine folic acid placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine 5mg x2 tablets + amlodipine folic acid (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) Amlodipine besylate And Folic Acid Amlodipine folic acid 5.8mg x1 tablet + amlodipine (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine folic acid tablets, amlodipine placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) Amlodipine placebo Amlodipine folic acid 5.8mg x1 tablet + amlodipine (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine folic acid tablets, amlodipine placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) 5-MTHF Placebos Amlodipine folic acid 5.8mg x1 tablet + amlodipine (dummy) x1 tablet + 5-MTHF (dummy) x2 tablets, taken orally, in the morning after waking up. Amlodipine folic acid tablets, amlodipine placebos, and 5-MTHF placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF (dummy) x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) + 5-MTHF (0.4mg/d) Amlodipine besylate And Folic Acid Amlodipine folic acid 5.8mg x1 tablet + 5-methyltetrahydrofolate 0.2mg x2 tablets + amlodipine (dummy) x1 tablet, taken orally, in the morning after waking up. Amlodipine folic acid tablets, 5-MTHF, and amlodipine placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF, 0.2mg x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) + 5-MTHF (0.4mg/d) 5-methyltetrahydrofolate (5-MTHF) Amlodipine folic acid 5.8mg x1 tablet + 5-methyltetrahydrofolate 0.2mg x2 tablets + amlodipine (dummy) x1 tablet, taken orally, in the morning after waking up. Amlodipine folic acid tablets, 5-MTHF, and amlodipine placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF, 0.2mg x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day). Amlodipine folic acid (5.8mg/d) + 5-MTHF (0.4mg/d) Amlodipine placebo Amlodipine folic acid 5.8mg x1 tablet + 5-methyltetrahydrofolate 0.2mg x2 tablets + amlodipine (dummy) x1 tablet, taken orally, in the morning after waking up. Amlodipine folic acid tablets, 5-MTHF, and amlodipine placebos are provided in aluminum-plastic blister plate. Each package includes 100 days of treatment drug (including 10 extra days of treatment for the follow-up window). A package of medication consists of 50 plates, each plate includes a total of 8 tablets arranged as follows: amlodipine folic acid 5.8mg x2 tablets + amlodipine (dummy) x2 tablets + 5-MTHF, 0.2mg x4 tablets. Affixed to the package is the randomized treatment drug label (400 tablets/package, 4 tablets/day).
- Primary Outcome Measures
Name Time Method First ischemic stroke By the end of the fifth year of the study The primary aim of the trial is to determine whether amlodipine folic acid tablets (including Group B and Group C), compared to amlodipine alone (Group A), can further reduce the risk of first ischemic stroke among eligible participants with hypertension and the MTHFR 677 TT genotype.
- Secondary Outcome Measures
Name Time Method First ischemic stroke (for refined treatment group comparisons) By the end of the fifth year of the study We will examine whether there exist significant differences in efficacy in reducing the risk of first ischemic stroke between the following pairs of treatment groups:
Group B vs. Group A
Group C vs. Group A
Group B vs. Group CFirst stroke (ischemic and hemorrhagic) By the end of the fifth year from baseline We will examine whether there exist significant differences in efficacy in reducing the risk of first stroke between the following pairs of treatment groups:
Groups B + C vs. Group A
Group B vs. Group A
Group C vs. Group A
Group B vs. Group CComposite cardiovascular endpoint (first non-fatal stroke, first non-fatal myocardial infarction, cardiovascular death) By the end of the fifth year from baseline We will examine whether there exist significant differences in efficacy in reducing the risk of composite cardiovascular endpoint between the following pairs of treatment groups:
Groups B + C vs. Group A
Group B vs. Group A
Group C vs. Group A
Group B vs. Group CKidney outcomes By the end of the fifth year from baseline 1. The primary kidney outcome is composite kidney outcome, defined as: (1) a decrease in eGFR of 30% or more and to a level of less than 60 mL/min/1.73 m2 if the baseline eGFR is 60 mL/min/1.73 m2 or more, or (2) a decrease in eGFR of 50% or more if the baseline eGFR is less than 60 mL/min/1.73 m2, or (3) end-stage kidney disease (ESKD) (eGFR \<15 mL/min/1.73m2 or dialysis or kidney transplantation).
2. Secondary kidney outcomes: (1) eGFR decline ≥40% from baseline, or end-stage kidney disease; (2) annual rate of relative decline in eGFR; (3) Incidence of proteinuria, or progression of proteinuria.
We will examine whether there exist significant differences in treatment efficacy on the above kidney endpoints between the following pairs of treatment groups:
Groups B + C vs. Group A
Group B vs. Group A
Group C vs. Group A
Group B vs. Group CFirst hemorrhagic stroke By the end of the fifth year from baseline We will examine whether amlodipine folic acid tablets (including Groups B and C), compared to amlodipine alone (Group A), show significantly greater efficacy in preventing first hemorrhagic stroke.
First myocardial infarction By the end of the fifth year from baseline We will examine whether amlodipine folic acid tablets (including Groups B and C), compared to amlodipine alone (Group A), show significantly greater efficacy in preventing first myocardial infarction.
First coronary revascularization (coronary artery bypass grafting [CABG] or percutaneous coronary intervention [PCI]) By the end of the fifth year from baseline We will examine whether amlodipine folic acid tablets (including Groups B and C), compared to amlodipine alone (Group A), show significantly greater efficacy in preventing first coronary revascularization.
Cardiovascular death By the end of the fifth year from baseline We will examine whether amlodipine folic acid tablets (including Groups B and C), compared to amlodipine alone (Group A), show significantly greater efficacy in preventing cardiovascular death.
Trial Locations
- Locations (20)
First Affillated Hospital of Bengbu Medical University
🇨🇳Bengbu, Anhui, China
Bozhou People's Hospital
🇨🇳Bozhou, Anhui, China
Chizhou People's Hospital
🇨🇳Chizhou, Anhui, China
Taihe County People's Hospital
🇨🇳Fuyang, Anhui, China
Peking University First Hospital
🇨🇳Beijing, Beijing, China
Yangjiang People's Hospital
🇨🇳Yangjiang, Guangdong, China
The Affiliated Hospital of Guizhou Medical University
🇨🇳Guiyang, Guizhou, China
The First Affiliated Hospital of Hunan University of Medicine
🇨🇳Huaihua, Hunan, China
Loudi Central Hospital
🇨🇳Loudi, Hunan, China
Lianyungang Oriental Hospital
🇨🇳Lianyungang, Jiangsu, China
The First People's Hospital of Lianyungang
🇨🇳Lianyungang, Jiangsu, China
The Second People's Hospital of Lianyungang
🇨🇳Lianyungang, Jiangsu, China
Yancheng First People's Hospital
🇨🇳Yancheng, Jiangsu, China
The First Affiliated Hospital of Gannan Medical University
🇨🇳Ganzhou, Jiangxi, China
Second Affiliated Hospital of Nanchang University
🇨🇳Nanchang, Jiangxi, China
Weinan Central Hospital
🇨🇳Weinan, Shaanxi, China
Tengzhou Central People's Hospital
🇨🇳Zaozhuang, Shandong, China
Chengdu Fifth People's Hospital
🇨🇳Chengdu, Sichuan, China
Deyang People's Hospital
🇨🇳Deyang, Sichuan, China
The Affiliated Hospital of Southwest Medical University
🇨🇳Luzhou, Sichuan, China