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NCT04680221 · ClinicalTrials.gov registry record · Phase 4
Stopping Opioid Overuse in Obstetrics to Halt Exposure Trial
A Phase 4 study of Pain, Postoperative and Opioid Use, sponsored by University of Missouri, Kansas City.
- Active
- Registry status
- Phase 4
- Development phase
- 97
- Enrollment target
- 1
- Study location
NCT04680221 is a Phase 4 study of Pain, Postoperative and Opioid Use that is active but no longer recruiting, run by University of Missouri, Kansas City. The registered enrollment target is 97 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04680221, a Phase 4 study of Pain, Postoperative and Opioid Use, is active but no longer recruiting, sponsored by University of Missouri, Kansas City.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 4
- Development phase
- 97 participants
- Enrollment target
- 1
- Study location
Study Summary
As the opioid epidemic continues on, more research is needed on multi-modal approaches to decrease opioid exposure after common procedures. The aim of this study is to investigate the role of a transverses abdominis block using liposome bupivacaine suspension in reducing use of opioid medications through post-operative day 7. The study is a proposed double-blind, randomized controlled trial.
Conditions Studied
Interventions
- DRUG Liposomal bupivacaine
- PROCEDURE TAP block
- DRUG Deposition of saline
Study Locations (1)
Missouri
- Truman Medical Center - Lakewood - Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 97 participants |
| Start Date | 2021-03-01 |
| Est. Completion | 2025-06-01 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04680221
The ClinicalTrials.gov registry entry for NCT04680221 describes a study currently listed as active not recruiting, categorized as Phase 4. The registered enrollment target is 97 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (64% lower). The listed sponsor is University of Missouri, Kansas City, which has 33 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 3 interventions - of which Liposomal bupivacaine is the first listed.
NCT04680221 reports 1 study location spanning 1 distinct geographic area - top geographies include Missouri.
Frequently Asked Questions
What is clinical trial NCT04680221 about?
NCT04680221 is a clinical study titled "Stopping Opioid Overuse in Obstetrics to Halt Exposure Trial". As the opioid epidemic continues on, more research is needed on multi-modal approaches to decrease opioid exposure after common procedures. The aim of this study is to investigate the role of a transverses abdominis block using liposome bupivacaine suspension in reducing use of opioid medications th...
What is the current status of trial NCT04680221?
This trial is currently active not recruiting. It is a Phase 4 study. The enrollment target is 97 participants. The study started on 2021-03-01. Estimated completion is 2025-06-01.
What conditions does trial NCT04680221 study?
This clinical trial studies the following conditions: Pain, Postoperative, Opioid Use.
What interventions are being tested in trial NCT04680221?
The interventions under investigation include: Liposomal bupivacaine (DRUG), TAP block (PROCEDURE), Deposition of saline (DRUG).
Who is sponsoring clinical trial NCT04680221?
This trial is sponsored by University of Missouri, Kansas City, which has 33 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04680221 being conducted?
This trial has 1 study location across Missouri. 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
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.