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NCT01271855 · ClinicalTrials.gov registry record · Phase 4
Assessing Maternal Post-partum Pain With Suppositories
A Phase 4 study, sponsored by Loyola University.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
NCT01271855: Completed Phase 4 study, sponsored by Loyola University.
NCT01271855 is a Phase 4 study that has completed, run by Loyola University. The registered enrollment target is 100 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01271855, a Phase 4 study, has completed, sponsored by Loyola University.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
Study Summary
This trial will evaluate whether the routine use of belladonna/opium (B\&O) suppositories improve patients' self-reported pain control in the first 24-hours after delivery.
Primary Outcome
The primary outcome is pain measured at 24-hours after delivery. Patients will be asked to report a Visual Analog Scale (VAS) pain score at 24-hours after delivery. This scale ranges from 0 to 10 (0=no pain and 10=worst pain).
Interventions
- DRUG Glycerin Suppository
- DRUG Belladonna and opioid suppository
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2009-07-22 |
| Est. Completion | 2011-09-29 |
| Phase | Phase 4 |
What the finished NCT01271855 record still lists
NCT01271855 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (81% lower).
The record links to 0 conditions, and to 2 interventions - of which Glycerin Suppository is the first listed.
NCT01271855 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01271855 about?
NCT01271855 is a clinical study titled "Assessing Maternal Post-partum Pain With Suppositories". This trial will evaluate whether the routine use of belladonna/opium (B\&O) suppositories improve patients' self-reported pain control in the first 24-hours after delivery.
What is the current status of trial NCT01271855?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2009-07-22. Estimated completion is 2011-09-29.
What interventions are being tested in trial NCT01271855?
The interventions under investigation include: Glycerin Suppository (DRUG), Belladonna and opioid suppository (DRUG).
Who is sponsoring clinical trial NCT01271855?
This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01271855's enrollment target sits among peer trials
100 770th of 2000 higher than 1,148 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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