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NCT01707251 · ClinicalTrials.gov registry record · Phase 4
Intravenous Ibuprofen for Laparoscopic Bariatric Surgery
A Phase 4 study, sponsored by Jacobi Medical Center.
- Completed
- Registry status
- Phase 4
- Development phase
- 100
- Enrollment target
NCT01707251: Completed Phase 4 study, sponsored by Jacobi Medical Center.
NCT01707251 is a Phase 4 study that has completed, run by Jacobi Medical Center. 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
NCT01707251, a Phase 4 study, has completed, sponsored by Jacobi Medical Center.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 100 participants
- Enrollment target
Study Summary
Primary objective of this study is to test hypothesis that IV ibuprofen decreases 24 hours morphine requirement using IV PCA in patients after laparoscopic bariatric surgery. Secondary objective is to determine if it decreases respiratory depression measured using RD, improves area under curve (AUC) for pain scores at rest (AUCr) and with cough (AUCa) and pressure pain threshold (PPT) (important for mobilization). Tertiary objective is to compare incidence of nausea/vomiting, sedation, itching, blood transfusion, over sedation, urinary retention, GI or surgical bleeding, renal dysfunction, time to clears and baseline activity in ibuprofen and control groups.
Primary Outcome
Will test if IV ibuprofen decrease postoperative morphine requirement.
Interventions
- DRUG Saline
- DRUG Intravenous Ibuprofen
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2012-10 |
| Est. Completion | 2015-03 |
| Phase | Phase 4 |
What the finished NCT01707251 record still lists
NCT01707251 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 Saline is the first listed.
NCT01707251 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01707251 about?
NCT01707251 is a clinical study titled "Intravenous Ibuprofen for Laparoscopic Bariatric Surgery". Primary objective of this study is to test hypothesis that IV ibuprofen decreases 24 hours morphine requirement using IV PCA in patients after laparoscopic bariatric surgery. Secondary objective is to determine if it decreases respiratory depression measured using RD, improves area under curve (AUC)...
What is the current status of trial NCT01707251?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 100 participants. The study started on 2012-10. Estimated completion is 2015-03.
What interventions are being tested in trial NCT01707251?
The interventions under investigation include: Saline (DRUG), Intravenous Ibuprofen (DRUG).
Who is sponsoring clinical trial NCT01707251?
This trial is sponsored by Jacobi Medical Center, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01707251'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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