Trials / Unknown
UnknownNCT06264622
ABG+/GarlACE Effects on Cardiovascular Risk Factors in Subjects With Grade I Hypertension
Dose Response Study of the Effects of a Daily Supplementation With a Black Garlic Extract, ABG+/GarlACE on Cardiovascular Disease Risk Factors in Subjects With Grade I Hypertension
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 180 (estimated)
- Sponsor
- Universitat de Lleida · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
The goal of this clinical trial is to evaluate the dose response effect on cardiovascular disease risk factors of a Black Garlic Extract in subjects with Grade I Hypertension. The main questions it aims to answer are: * If the reduction in blood pressure (systolic and diastolic) is in a dose-response manner * If the changes in lipid profile are in a dose-response manner Participants will be randomly assign to a low dose (250 mg/day), high dose (600 mg/day) or placebo of a standardized Garlic Extract (ABG+/GarlACE) during 12 weeks
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Low dose | 2 tablets per day during the morning for 12 weeks. |
| DIETARY_SUPPLEMENT | High dose | 2 tablets per day during the morning for 12 weeks. |
| DIETARY_SUPPLEMENT | Placebo | 2 tablets per day during the morning for 12 weeks. |
Timeline
- Start date
- 2024-02-26
- Primary completion
- 2024-10-31
- Completion
- 2024-12-31
- First posted
- 2024-02-20
- Last updated
- 2024-02-20
Locations
1 site across 1 country: Spain
Source: ClinicalTrials.gov record NCT06264622. Inclusion in this directory is not an endorsement.