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NCT02400580 · ClinicalTrials.gov registry record · Phase 4
IV Acetaminophen for Postoperative Pain Analgesia After Laparoscopic Hysterectomy
A Phase 4 study of Pain, sponsored by University of Pittsburgh.
- Completed
- Registry status
- Phase 4
- Development phase
- 183
- Enrollment target
- 1
- Study location
NCT02400580 is a Phase 4 study of Pain that has completed, run by University of Pittsburgh. The registered enrollment target is 183 participants, below the 304-participant average among 374 other Pain trials with a reported enrollment target (40% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02400580, a Phase 4 study of Pain, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 183 participants
- Enrollment target
- 1
- Study location
Study Summary
The objective of this study is to quantify the change in post-operative pain scores and narcotic requirements in women receiving pre and post-operative IV acetaminophen compared to placebo in women undergoing laparoscopic hysterectomy.
Conditions Studied
Interventions
- DRUG placebo
- DRUG IV acetaminophen
Study Locations (1)
Pennsylvania
- Magee Womens Hospital - Pittsburgh
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 183 participants |
| Start Date | 2015-02 |
| Est. Completion | 2016-09 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02400580
The ClinicalTrials.gov registry entry for NCT02400580 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 183 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 304-participant average among 374 other Pain trials with a reported enrollment target (40% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 2 interventions - of which placebo is the first listed.
NCT02400580 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT02400580 about?
NCT02400580 is a clinical study titled "IV Acetaminophen for Postoperative Pain Analgesia After Laparoscopic Hysterectomy". The objective of this study is to quantify the change in post-operative pain scores and narcotic requirements in women receiving pre and post-operative IV acetaminophen compared to placebo in women undergoing laparoscopic hysterectomy.
What is the current status of trial NCT02400580?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 183 participants. The study started on 2015-02. Estimated completion is 2016-09.
What conditions does trial NCT02400580 study?
This clinical trial studies the following conditions: Pain.
What interventions are being tested in trial NCT02400580?
The interventions under investigation include: placebo (DRUG), IV acetaminophen (DRUG).
Who is sponsoring clinical trial NCT02400580?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02400580 being conducted?
This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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