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Randomised controlled study of 'physiological' peritoneal dialysis solutions

Randomised controlled study of 'physiological' peritoneal dialysis solutions

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN37099489
Enrollment
131
Registered
2007-09-28
Start date
2004-01-29
Completion date
Unknown
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urological and Genital Diseases: Peritoneal dialysis Urological and Genital Diseases Peritoneal dialysis

Interventions

"Physiological" (pH neutral) versus "standard" (low pH) dialysate solution

Sponsors

Record Provided by the NHSTCT Register - 2007 Update - Department of Health
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients selected to use a PD system that has physiological and standard solutions available

Exclusion criteria

Exclusion criteria: 1. Patients unable to provide informed consent 2. Patients where the use of a certain solution is indicated or contra-indicated for medical reasons (eg known allergy)

Design outcomes

Primary

MeasureTime frame
Patients using physiological solutions will have lower peritonitis rate than control group.

Secondary

MeasureTime frame
1. Patients using physiological solutions will have better preservation of residual kidney function 2. Patients using physiological solutions will have smaller changes in peritoneal membrane function assessed by PET than control group 3. Patients using physiological solutions will have reduced composite end-point of mortality and PD failure defined by transfer to HD in patients using physiological solutions

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026