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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

TypeNameDescription
DRUGHydrochlorothiazide 25mg once per dayThiazides 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.

Blood Pressure Control With Thiazide Diuretics in Peritoneal Dialysis Patients (NCT07271420) · Clinical Trials Directory