Trials / Terminated
TerminatedNCT05370599
Hypertension in Young Adults Trial
- Status
- Terminated
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 36 (actual)
- Sponsor
- University of California, San Francisco · Academic / Other
- Sex
- All
- Age
- 18 Years – 40 Years
- Healthy volunteers
- Accepted
Summary
This is a pilot randomized controlled trial which will test the effect of 3 different anti-hypertensive agents and 3 different strategies of engaging young adults in home blood pressure monitoring on blood pressure control, with secondary outcomes focused on quality of life and adverse events.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Anti-hypertensive agent: amlodipine | Patients with hypertension will be randomly assigned to be treated with amlodipine, chlorthalidone, or losartan. All drugs will be initiated at the lowest dose and uptitrated as needed to achieve standard BP targets. |
| DRUG | Anti-hypertensive agent: Chlorthalidone | Patients with hypertension will be randomly assigned to be treated with amlodipine, chlorthalidone, or losartan. All drugs will be initiated at the lowest dose and uptitrated as needed to achieve standard BP targets. |
| DRUG | Anti-hypertensive agent: Losartan | Patients with hypertension will be randomly assigned to be treated with amlodipine, chlorthalidone, or losartan. All drugs will be initiated at the lowest dose and uptitrated as needed to achieve standard BP targets. |
| DEVICE | Home BP monitoring with cuffed device | Patients will be randomized to monitor their blood pressure either with a BP cuffed device alone, versus with either or use of a BP monitoring patch or BP monitoring watch. |
| DEVICE | Home BP monitoring with cuffed device + BP patch | Patients will be randomized to monitor their blood pressure either with a BP cuffed device alone, versus with either or use of a BP monitoring patch or BP monitoring watch. |
| DEVICE | Home BP monitoring with cuffed device + BP watch | Patients will be randomized to monitor their blood pressure either with a BP cuffed device alone, versus with either or use of a BP monitoring patch or BP monitoring watch. |
Timeline
- Start date
- 2022-04-15
- Primary completion
- 2026-01-07
- Completion
- 2026-01-07
- First posted
- 2022-05-11
- Last updated
- 2026-01-13
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05370599. Inclusion in this directory is not an endorsement.