Trials / Recruiting
RecruitingNCT07271420
Blood Pressure Control With Thiazide Diuretics in Peritoneal Dialysis Patients
- Status
- Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- Chinese University of Hong Kong · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the blood pressure lowering effects of thiazide diuretics in patients on peritoneal dialysis
Detailed description
This prospective, single-center treatment-withdrawal crossover study enrolled 10 patients on chronic peritoneal dialysis (PD) and uncontrolled hypertension (SBP \>140 mmHg and/or DBP \>90 mmHg). Following written informed consent, participants entered the treatment arm, receiving oral hydrochlorothiazide once daily on top of their standard of treatment for 90 days. This was followed by a 14-day washout period, after which participants entered a 90-day control period.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Hydrochlorothiazide 25mg once per day | Thiazides diuretics |
Timeline
- Start date
- 2020-01-01
- Primary completion
- 2026-12-31
- Completion
- 2027-06-30
- First posted
- 2025-12-09
- Last updated
- 2025-12-09
Locations
1 site across 1 country: Hong Kong
Source: ClinicalTrials.gov record NCT07271420. Inclusion in this directory is not an endorsement.