Clinical Trials Directory

Trials / Completed

CompletedNCT07386210

Antihypertensive Effects of Rosmarinus Officinalis L. Infusion

Antihypertensive Effects of Rosmarinus Officinalis L. Infusion Supplements in Male Patients With Mild Hypertension : A Randomized Double-Blind Placebo-Controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
54 (actual)
Sponsor
awatef Sassi · Academic / Other
Sex
Male
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study assessed the antihypertensive effect of rosemary tea through a placebo-controlled clinical study, angiotensin-converting enzyme (ACE) inhibition analysis, and in silico evaluation of interactions between rosemary bioactive compounds and the AT1R (Angiotensin II Type 1 Receptor). A randomized, double-blind, placebo-controlled trial was conducted in 54 male patients with mild hypertension. Participants were assigned to receive either rosemary infusion (n = 27) or placebo (n = 23) for 45 days. Ambulatory blood pressure monitoring wass used to evaluate blood pressure parameters. Serum ACE activity was measured at baseline and after the intervention using FAPGG hydrolysis. Molecular docking simulations were performed using the Dock 4.2 software.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTRosemary extract infusionInfusion prepared from 2g of rosemary leaves Administered orally, 1 cup (100 mL) per day Duration: 6 weeks
DIETARY_SUPPLEMENTPlaceboInfusion with color and taste similar to rosemary, without active extract Administered orally, 1 cup (100 mL) per day Duration: 6 weeks

Timeline

Start date
2023-03-20
Primary completion
2025-08-28
Completion
2025-08-29
First posted
2026-02-04
Last updated
2026-02-04

Locations

2 sites across 1 country: Tunisia

Source: ClinicalTrials.gov record NCT07386210. Inclusion in this directory is not an endorsement.