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临床试验/NCT06246396
NCT06246396招募中4 期

Antihypertensive Mechanisms of Minocycline in Resistant Hypertension: Role of the Gut Microbiota-brain-immune Axis

University of Florida1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2025年1月8日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
120
试验地点
1
主要终点
Gut microbiome

研究概览

简要总结

The goal of this clinical trial is to learn about the mechanisms by which minocycline effect blood pressure in individuals with treatment-resistant hypertension. The main questions it aims to answer are:

  • To what extent does minocycline lower blood pressure?
  • Are such blood pressure effects mediated through changes in gut microbiota, gut leakiness, systemic inflammation, neuroinflammation, or some combination of these?

Participants will be randomly assigned to treatment with minocycline or placebo, treated daily for 3 months, to evaluate these questions.

详细描述

One hundred twenty patients with treatment-resistant hypertension will be enrolled. A total of 34 patients (17 from each treatment arm), who are participants in the main study, will also be enrolled in a substudy that includes neuroimaging. The study will last 3 months, and will include 3 visit time points (screening, randomization visit, 3-month follow-up visit).

Participants will be randomly assigned, in a 1:1 allocation, to minocycline 100 mg twice per day, or matching placebo, each provided by the study, and investigators will be blinded to treatment assignment.

At the baseline and 3-month follow-up visit, subjects will undergo:

  • A comprehensive medical history and examination, including assessment of antihypertensive treatment history
  • A series of behavioral activity questionnaires
  • Blood tests (plasma renin activity, aldosterone, catecholamines, serum creatinine, lipid panel, hemoglobin a1c, as well as various biomarkers of immune and inflammatory activity, and gut leakiness markers)
  • Urine/saliva tests for antihypertensive adherence
  • Gut microbiota profiling via whole metagenomic sequencing of stool samples
  • Blood pressure (BP) measurement, including unattended office BP and 24-hour ambulatory BP

Subjects enrolled in the neuroimaging substudy will also have PET/MR imaging performed at each visit. Neuroimaging activities will take place at Emory University in Atlanta, GA.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥18 years
  • Uncontrolled TRH, defined as uncontrolled blood pressure (mean 24-hour ambulatory systolic BP ≥125 mm Hg or diastolic BP ≥80 mm Hg) while being adherent to a stable (no changes in ≥14 days prior) antihypertensive regimen of 3 or more drugs, including an adequately dosed diuretic or unable to tolerate a diuretic.
  • The participant agrees to have all study procedures performed

排除标准

  • Known hypersensitivity or contraindication to minocycline or other tetracyclines
  • Recent (≤3 months prior), ongoing, or expected use of oral antibiotics
  • Estimated glomerular filtration rate (eGFR) of <45mL/min/1.73m2, using the MDRD equation
  • Known secondary hypertension
  • History of hypertensive crisis, defined as any in-patient hospitalizations for hypertensive crisis/emergency within the past year
  • History of orthostatic hypotension, defined as two or more episode(s) of orthostatic hypotension (reduction of SBP of >20 mm Hg or DBP of >10 mm Hg within 3 minutes of standing) in the past year
  • History of myocardial infarction, unstable angina, syncope, or cerebrovascular accident in prior 6 months
  • Evidence of alcoholism or drug abuse
  • Severe comorbid conditions (i.e., neoplasms or HIV positive or AIDS)
  • Current pregnancy or anticipated pregnancy during the study.

研究组 & 干预措施

Minocycline Hydrochloride

Experimental

Minocycline hydrochloride 100 mg, administered twice daily for 3 months

干预措施: Minocycline Hydrochloride (Drug)

Placebo

Placebo Comparator

Placebo administered twice daily for 3 months

干预措施: Placebo (Drug)

结局指标

主要结局

Gut microbiome

时间窗: 3 months

Change in butyrate-producing gene abundance

24-h systolic blood pressure

时间窗: 3 months

Change in mean 24-hour ambulatory systolic blood pressure

Gut inflammation and leakiness

时间窗: 3 months

Change in gut-homing inflammatory T-helper cells

Neuroinflammation

时间窗: 3 months

Change in \[18F\]FEPPA radiotracer uptake on PET/MR imaging

次要结局

  • 24-h heart rate(3 months)
  • Mucin-degrading gene abundance(3 months)
  • IgA+ coated plasma cells(3 months)
  • Gut leakiness markers(3 months)
  • 24-h diastolic blood pressure(3 months)
  • Adverse Events(3 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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