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NCT03391284 · ClinicalTrials.gov registry record · NA
Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery
A NA study of Postoperative Pain, sponsored by Scripps Health.
- Completed
- Registry status
- NA
- Development phase
- 75
- Enrollment target
- 2
- Study locations
NCT03391284: Completed NA study of Postoperative Pain, sponsored by Scripps Health.
NCT03391284 is a NA study of Postoperative Pain that has completed, run by Scripps Health. The registered enrollment target is 75 participants, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (68% lower). The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03391284, a NA study of Postoperative Pain, has completed, sponsored by Scripps Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 75 participants
- Enrollment target
- 2
- Study locations
Study Summary
Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasive benign gynecologic surgery. Primary outcome: • Difference in postoperative pain comparing preemptive use of PO versus IV acetaminophen o Mean Visual analog Scale (VAS) scores will be compared between the intervention group (PO acetaminophen) and the control group (IV acetaminophen). Secondary outcomes: * Difference in postoperative analgesic use between groups o Narcotics, NSAIDs * Difference in postoperative N/V between groups o Patient rated measure - none, mild, moderate, severe * Cost comparison between drugs
Primary Outcome
Pain level 2 hours post treatment
Conditions Studied
Interventions
- DRUG Acetaminophen
- DRUG acetominophen
Study Locations (2)
California
- Scripps Clinic - San Diego
- Scripps Clininc Dept of Ob/Gyn - San Diego
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 75 participants |
| Start Date | 2016-02 |
| Est. Completion | 2018-02 |
| Phase | NA |
What the finished NCT03391284 record still lists
NCT03391284 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 75 participants, a relatively small participant target, below the 231-participant average among 120 other Postoperative Pain trials with a reported enrollment target (68% lower).
The record links to 1 condition, with Postoperative Pain appearing as the primary indexed condition, and to 2 interventions - of which Acetaminophen is the first listed.
NCT03391284 reports a single indexed study location in California.
Frequently Asked Questions
What is clinical trial NCT03391284 about?
NCT03391284 is a clinical study titled "Oral vs Intravenous Acetominophen for Postoperative Pain in Minimally Invasive Gynecologic Surgery". Hypothesis: Postoperative pain will be equivalent in patients receiving preemptive oral acetaminophen as compared to patients receiving preemptive intravenous acetaminophen following minimally invasive benign gynecologic surgery. Primary outcome: • Difference in postoperative pain comparing preemp...
What is the current status of trial NCT03391284?
This trial is currently completed. It is a NA study. The enrollment target is 75 participants. The study started on 2016-02. Estimated completion is 2018-02.
What conditions does trial NCT03391284 study?
This clinical trial studies the following conditions: Postoperative Pain.
What interventions are being tested in trial NCT03391284?
The interventions under investigation include: Acetaminophen (DRUG), acetominophen (DRUG).
Who is sponsoring clinical trial NCT03391284?
This trial is sponsored by Scripps Health, which has 30 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03391284 being conducted?
This trial has 2 study locations across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Pain
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT03391284's enrollment target sits among peer trials
75 77th of 120 higher than 41 of 120 other Postoperative Pain trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Postoperative Pain 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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