A study to evaluate how well OxyjunTM improves Heart function as well as Work performance in Individuals with Metabolic health issues.
- Conditions
- Health Condition 1: E889- Metabolic disorder, unspecified
- Registration Number
- CTRI/2024/08/072478
- Lead Sponsor
- Vedic Lifesciences Pvt. Ltd.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1.Individuals of either sex, aged more than equal to 45 to less than equal to 70 years at the time of screening with BMI more than equal to 25 kg/metre square to less than equal to 34.9 kg/metre square.
2.Individuals with normal to high blood pressure (BP) [systolic BP more than equal to 120 mmHg and less than equal to 159 mmHg and/or diastolic BP more than equal to 80 mmHg and less than equal to 89 mmHg].
3.Individuals with waist circumference more than equal to 40 inches for men or 35 inches for women.
4.Individuals with normal to mildly deranged ‘Left ventricular ejection’ as per American College of Cardiology: LVEF more than equal to 45% and less than equal to 55%.
5. Fasting glucose level of more than equal to 110 mg/dL and less than equal to 160 mg/dL (without medication or with maximum 500 mg of daily dose of Metformin).
6.Individuals with Aspartate aminotransaminase (AST) and Alanine transaminase (ALT) within 2 times upper normal limit (ULN).
7.Individuals with 1.5 x Upper Limit of Normal of Creatinine.
8.Individuals having following values of haemoglobin:
a) Female - more than equal to 11 mg/dl.
b) Male - more than equal to 12 mg/dl.
9. Individuals with thyroid stimulating hormone (TSH) levels between the 0.27 IU/ml and 5 IU/ml both values included.
10. Individuals who demonstrate their willingness to participate in the study and comply with the study procedures and required visits.
11. Willing to abstain from caffeine for 12 hours prior to study visit.
12. Willing to abstain from alcohol and related products consumption for 48 hours prior to study visits.
13. Must be literate, having the ability to understand, complete the study-based questionnaires, requirements and sign a written informed consent form, which must be completed prior to study specific requirements being performed.
1. History or presence of clinically significant renal, hepatic, endocrine, biliary, gastrointestinal, pancreatic or neurologic disorders that, in the judgement of the investigator, would interfere with the individuals ability to provide informed consent, comply with the study protocol, or put the individual at undue risk.
2. Using Omega fish oil supplements, anticonvulsants, Coenzyme Q10, Vitamin K2, proton pump inhibitors, loop diuretics, anticoagulants, barbiturates, anti-epileptic medications and any herbal supplements (e.g. flax seeds, chia seeds).
3. Chronic use of anti-inflammatory medications (more than equal to 5 tablets/20 days in last 3 months).
4. Individuals having a history of smoking or currently smoking and also using any form of smokeless tobacco.
5. High-risk drinking as defined by consumption of 4 or more drinks of alcohol containing beverages on any day or 10 or more drinks of alcohol containing beverages per week for women and 5 or more drinks of alcohol containing beverages on any day or 14 or more drinks of alcohol containing beverages per week for men.
6. Individuals unable to walk.
7. Individuals with a history of chronic caffeine use with more than 3 cups of caffeinated beverage/ day.
8. Individuals who have any other disease or condition, or are using any medication, that in the judgment of the investigator would put him/her at unacceptable risk for participation in the study or may interfere with evaluations in the study or noncompliance with treatment or visits.
9. Females who are pregnant/planning to be pregnant/lactating or taking any oral contraceptives.
10. Females undergoing hormone replacement treatments.
11. Peri- or post-menopausal females having less then equal to 1 year of irregular or complete absence of menstrual cycle.
12. Those unwilling to abstain from other dietary supplements or medication (e.g. Hepatoprotective agents and complementary and alternative medicine).
13. Have participated in a study of an investigational product 90 days prior to the screening.
14. Individuals with known or suspected hypersensitivity or intolerance to Investigational product.
15. Individuals who are unable to comply with study requirements.
16. Individuals with history of autoimmune disorders.
17. Individuals with history of immunocompromised status.
18. Any clinical signs or symptoms that in the opinion of investigator, can jeopardize the outcome of the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the effect of 8-week oral consumption of OxyjunTM on left ventricular function as evaluated by Left ventricle ejection fraction (LVEF).Timepoint: Screening, Day 28, Day 56
- Secondary Outcome Measures
Name Time Method To evaluate the effect of 8-week oral consumption of Oxyjun TM on Responder to the product as assessed by the number of the participant having LVEF more than equal to 5 units increase.Timepoint: Screening, Day 28, and Day 56;To evaluate the effect of 8-week oral consumption of Oxyjun TM on Cardiac pumping capacity as evaluated by the ventricular stroke volume and cardiac output.Timepoint: Screening, Day 28, and Day 56;To evaluate the effect of 8-week oral consumption of Oxyjun TM on Cardiac risk as assessed by the NT-Pro BNPTimepoint: Day 0 and Day 56;To evaluate the effect of 8-week oral consumption of Oxyjun TM on Physical activity as assessed by IPAQ questionnaire.Timepoint: Day 0, Day 28 and Day 56;To evaluate the effect of 8-week oral consumption of OxyjunTM on Work Productivity as assessed by the Work Productivity and Activity Impairment QuestionnaireTimepoint: Day 0, Day 28 and Day 56