Effectiveness of Potassium Supplement in Hypokalemic PD Patients: A Stratified Randomized Controlled Trial
Completed
- Conditions
- Hypokalemia in PD patientPeritonitisHospitalizationCardiovascular mortalityAll-cause mortalityHypokalemiaPeritoneal dialysisPeritonitisPotassium supplement
- Registration Number
- TCTR20190725004
- Lead Sponsor
- Faculty of medicine, Chulalongkorn university
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 192
Inclusion Criteria
1. End-stage kidney disease on peritoneal dialysis
2. Age 18-80 years.
3. Perform peritoneal dialysis more than 3 months.
4. Serum potassium less than 3.5 mEq/L from previous 6 months (Spotted serum potassium less than 3.5 mEq/L at least 3 visits or time-average serum potassium < 3.5 mEq/L)
Exclusion Criteria
1. Recent peritonitis within 3 months
2. Hybrid with hemodialysis
3. Gastrointestinal tract disease that cannot absorbed potassium supplement.
4. Liver cirrhosis CPS > C
5. Chronic infection/Malignancy/HIV/Pregnancy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Peritonitis 1 year Time to first peritonitis
- Secondary Outcome Measures
Name Time Method Cardiovascular mortality 1 year time to event analysis,All-cause mortality 1 year Time to event analysis,Hospitalization 1 year Time to event analysis,Technique failure 1 year Time to event analysis