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NCT01256541 · ClinicalTrials.gov registry record · Phase 1
Kristalose as Bowel Evacuant Prior to Colonoscopy
A Phase 1 study, sponsored by Benaroya Research Institute.
- Completed
- Registry status
- Phase 1
- Development phase
- 20
- Enrollment target
NCT01256541: Completed Phase 1 study, sponsored by Benaroya Research Institute.
NCT01256541 is a Phase 1 study that has completed, run by Benaroya Research Institute. The registered enrollment target is 20 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01256541, a Phase 1 study, has completed, sponsored by Benaroya Research Institute.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 20 participants
- Enrollment target
Study Summary
To determine whether Kristalose causes a significant increase in hydrogen and/or methane gas levels in patients requiring bowel evacuation, and also to determine the safety, efficacy, and patient preference of Kristalose as a bowel evacuant
Primary Outcome
To evaluate the primary objective of hydrogen and methane gas production as measured by: • Pre- and post-dose breath analysis for hydrogen and methane gas.
Interventions
- DRUG Kristalose
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2010-12 |
| Est. Completion | 2011-09 |
| Phase | Phase 1 |
What the finished NCT01256541 record still lists
NCT01256541 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (67% lower).
The record links to 0 conditions, and to 1 intervention - of which Kristalose is the first listed.
NCT01256541 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01256541 about?
NCT01256541 is a clinical study titled "Kristalose as Bowel Evacuant Prior to Colonoscopy". To determine whether Kristalose causes a significant increase in hydrogen and/or methane gas levels in patients requiring bowel evacuation, and also to determine the safety, efficacy, and patient preference of Kristalose as a bowel evacuant
What is the current status of trial NCT01256541?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 20 participants. The study started on 2010-12. Estimated completion is 2011-09.
What interventions are being tested in trial NCT01256541?
The interventions under investigation include: Kristalose (DRUG).
Who is sponsoring clinical trial NCT01256541?
This trial is sponsored by Benaroya Research Institute, which has 28 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01256541's enrollment target sits among peer trials
20 1629th of 2000 higher than 285 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other 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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