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NCT02155738 · ClinicalTrials.gov registry record · Phase 4
IV Acetaminophen for Postoperative Pain After Pelvic Organ Prolapse Repair
A Phase 4 study, sponsored by Halina M Zyczynski, MD.
- Completed
- Registry status
- Phase 4
- Development phase
- 204
- Enrollment target
NCT02155738: Completed Phase 4 study, sponsored by Halina M Zyczynski, MD.
NCT02155738 is a Phase 4 study that has completed, run by Halina M Zyczynski, MD. The registered enrollment target is 204 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02155738, a Phase 4 study, has completed, sponsored by Halina M Zyczynski, MD.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 204 participants
- Enrollment target
Study Summary
The purpose of this study is to determine whether preoperative IV Acetaminophen reduces postoperative pain and narcotic consumption in women undergoing surgical repair of pelvic organ prolapse.
Primary Outcome
VAS or Visual Analog Score is a quantitative measure, in this study, of pain that the subject is currently experiencing. The VAS is presented as a straight line which measures 100mm. The subject is instructed to mark an 'X' through this line reflecting the amount of pain that they are currently experiencing. Zero would indicate no pain, while '100' would indicate the most severe pain ever. Thus the total range for this scale would be 0-100 mm. Higher values indicate more pain; lower value indica
Interventions
- DRUG IV Acetaminophen
- DRUG IV normal saline
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 204 participants |
| Start Date | 2014-07 |
| Est. Completion | 2017-08-31 |
| Phase | Phase 4 |
What the finished NCT02155738 record still lists
NCT02155738 is an interventional study that assigns participants to a tested intervention. The registered 204 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 (61% lower).
The record links to 0 conditions, and to 2 interventions - of which IV Acetaminophen is the first listed.
NCT02155738 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02155738 about?
NCT02155738 is a clinical study titled "IV Acetaminophen for Postoperative Pain After Pelvic Organ Prolapse Repair". The purpose of this study is to determine whether preoperative IV Acetaminophen reduces postoperative pain and narcotic consumption in women undergoing surgical repair of pelvic organ prolapse.
What is the current status of trial NCT02155738?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 204 participants. The study started on 2014-07. Estimated completion is 2017-08-31.
What interventions are being tested in trial NCT02155738?
The interventions under investigation include: IV Acetaminophen (DRUG), IV normal saline (DRUG).
Who is sponsoring clinical trial NCT02155738?
This trial is sponsored by Halina M Zyczynski, MD, which has 3 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02155738's enrollment target sits among peer trials
204 402nd of 2000 higher than 1,598 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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