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NCT01798316 · ClinicalTrials.gov registry record · Phase 4
IV Acetaminophen for Postoperative Analgesia
A Phase 4 study, sponsored by Northwell Health.
- Terminated
- Registry status
- Phase 4
- Development phase
- 105
- Enrollment target
NCT01798316: Clinical Trial Phase 4 study, sponsored by Northwell Health.
NCT01798316 is a Phase 4 study that was terminated before completion, run by Northwell Health. The registered enrollment target is 105 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01798316, a Phase 4 study, was terminated before completion, sponsored by Northwell Health.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 105 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the use of IV acetaminophen for postoperative pain management after laparoscopic cholecystectomy to determine if its use to supplement standard of care pain management decreases the incidence of post-operative nausea and vomiting.
Primary Outcome
Number of participants with postoperative nausea and vomiting (PONV) will be recorded during PACU stay. PONV is defined as nausea intensity of 4 or higher on 0-10 numeric rating scale (NRS) and/or at least one episode of vomiting/retching.
Interventions
- DRUG Standard of Care
- DRUG IV Acetaminophen
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 105 participants |
| Start Date | 2013-03 |
| Est. Completion | 2015-09 |
| Phase | Phase 4 |
Why NCT01798316 stopped before completion
NCT01798316 is an interventional study that assigns participants to a tested intervention. The registered 105 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 (80% lower).
The record links to 0 conditions, and to 2 interventions - of which Standard of Care is the first listed.
NCT01798316 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01798316 about?
NCT01798316 is a clinical study titled "IV Acetaminophen for Postoperative Analgesia". The purpose of this study is to evaluate the use of IV acetaminophen for postoperative pain management after laparoscopic cholecystectomy to determine if its use to supplement standard of care pain management decreases the incidence of post-operative nausea and vomiting.
What is the current status of trial NCT01798316?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 105 participants. The study started on 2013-03. Estimated completion is 2015-09.
What interventions are being tested in trial NCT01798316?
The interventions under investigation include: Standard of Care (DRUG), IV Acetaminophen (DRUG).
Who is sponsoring clinical trial NCT01798316?
This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01798316's enrollment target sits among peer trials
105 749th of 2000 higher than 1,247 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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