To evaluate the effect of an interventional approach vs a conventional approach in incident peritoneal dialysis patients
Not Applicable
- Conditions
- Health Condition 1: null- Peritoneal Dialysis Patients
- Registration Number
- CTRI/2013/04/003561
- Lead Sponsor
- Baxter Evidence Council
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
1. Stable incident CKD stage 4 patients
2. Must be willing to give consent
Exclusion Criteria
1. Patient unwilling/unable to provide consent
2. Patient who are anuric or oliguric, at time of enrollment
3. Patient with life expectancy of less than 12 months
4. Pregnant or Lactating Women
5. Patient with history of likehood of poor compliance.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method