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NCT03801226 · ClinicalTrials.gov registry record · Early Phase 1
Zero Sodium Peritoneal Dialysate Protocol Pilot Study
A Early Phase 1 study, sponsored by Yale University.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 12
- Enrollment target
NCT03801226: Completed Early Phase 1 study, sponsored by Yale University.
NCT03801226 is a Early Phase 1 study that has completed, run by Yale University. The registered enrollment target is 12 participants, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (77% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03801226, a Early Phase 1 study, has completed, sponsored by Yale University.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
The following pilot study will be undertaken to determine the effects of use of a zero-sodium peritoneal dialysate solution (10% dextrose in sterile water) on sodium removal as compared to a standard peritoneal dialysis solution.
Primary Outcome
Protocol discontinuation will be defined by premature draining of the 10% dextrose peritoneal solution (or 4.25% standard PD solution) prior to the planned two hour drain.
Interventions
- DRUG Two-hour dwell with 10% dextrose in sterile water
- DRUG Two-hour dwell with Dianeal Low-Calcium with 4.25% Dextrose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2018-12-01 |
| Est. Completion | 2019-05-31 |
| Phase | Early Phase 1 |
What the finished NCT03801226 record still lists
NCT03801226 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 53-participant average among 2,764 other Early Phase 1 trials with a reported enrollment target (77% lower).
The record links to 0 conditions, and to 2 interventions - of which Two-hour dwell with 10% dextrose in sterile water is the first listed.
NCT03801226 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03801226 about?
NCT03801226 is a clinical study titled "Zero Sodium Peritoneal Dialysate Protocol Pilot Study". The following pilot study will be undertaken to determine the effects of use of a zero-sodium peritoneal dialysate solution (10% dextrose in sterile water) on sodium removal as compared to a standard peritoneal dialysis solution.
What is the current status of trial NCT03801226?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 12 participants. The study started on 2018-12-01. Estimated completion is 2019-05-31.
What interventions are being tested in trial NCT03801226?
The interventions under investigation include: Two-hour dwell with 10% dextrose in sterile water (DRUG), Two-hour dwell with Dianeal Low-Calcium with 4.25% Dextrose (DRUG).
Who is sponsoring clinical trial NCT03801226?
This trial is sponsored by Yale University, which has 1,492 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03801226's enrollment target sits among peer trials
12 1530th of 2000 higher than 401 of 2,000 other Early Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Early Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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