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Efficacy of resveratrol in patients with pre and first stage hypertension

Evaluation of efficacy of Resveratrol on hypertension, a randomized cross-over double- blinded placebo-controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201407078129N7
Enrollment
100
Registered
2014-08-15
Start date
2015-09-20
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension. High Blood pressure

Interventions

Intervention 1: The intervention group, Resveratrol ,99% pure(500 mg twice a day) for a period of one month. Intervention 2: The Control group, placebo ( 500 mg neutral cellulose, twice a day) for a p
Treatment - Drugs
Placebo
The intervention group, Resveratrol ,99% pure(500 mg twice a day) for a period of one month.
The Control group, placebo ( 500 mg neutral cellulose, twice a day) for a period of one month

Sponsors

Deputy of Research, Bushehr University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Pre-hypertensive(average of two times measurement with an interval of 15 minutes, diastolic and systolic blood pressure(80-89mmHg, 120-139 mmHg respectively) • Stage 1 hypertensive (average of two times measurement with an interval of 15 minutes (diastolic and systolic blood pressure 90-99 mmHg, 140-159 mmHg, respectively) • Male or Female • Age between 20 and 60-years • Ability to provide informed consent Exclusion Criteria:Approved or doubtful secondary hypertension; History of chronic or acute kidney Disease; History of heart failure; History of chronic or acute liver diseases; History of diabetes mellitus; History of prior cardiovascular events (Acute Myocardial Infarction, Cardiovascular diseases, Percutaneous Coronary Angioplasty or Coronary Artery Bypass Graft); Pregnancy or breast feeding;Blood arterial pressure >160/110

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Diastolic and systolic blood pressure. Timepoint: once in a week during intervention period. Method of measurement: A sphygmomanometer and Stethoscope will be used to measure the blood pressure, once in a week, and average of two times within 15 minutes will be recorded.;Added at 2015-04-16: Mean arterial pressure. Timepoint: Added at 2015-04-16: once in a week during intervention. Method of measurement: Added at 2015-04-16: systolic blood BP plus 2 times diastolic BP divided by 3.

Secondary

MeasureTime frame
PTT. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;SGOT. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Kits and ELISA method.;SGPT. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Kits and ELISA method.;GGT. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Kits and ELISA method.;ALP. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Kits and ELISA method.;TG. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;Cholesterol. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;LDL. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;HDL. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;Hematocrit. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: By Reputed kits.;Albumin. Timepoint: Before and after the first stage intervention, after one month washout and after one month of second stage intervention. Method of measurement: Auto-analyzer

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Movahed

Bushehr University of Medical Sciences

amovahed58@gmail.com ; amirali_19572yahoo.com+98 987712529198

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 13, 2026