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NCT04919317 · ClinicalTrials.gov registry record · Phase 2
Combination Dexamethasone and Bupivacaine Pain Control in Reduction Mammaplasty
A Phase 2 study of Pain, Postoperative and Mammaplasty, sponsored by Temple University.
- Completed
- Registry status
- Phase 2
- Development phase
- 56
- Enrollment target
- 1
- Study location
NCT04919317 is a Phase 2 study of Pain, Postoperative and Mammaplasty that has completed, run by Temple University. The registered enrollment target is 56 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (79% lower). The trial reports 1 study location across 1 state.
The verdict
NCT04919317, a Phase 2 study of Pain, Postoperative and Mammaplasty, has completed, sponsored by Temple University.
- COMPLETED
- Registry status
- Phase 2
- Development phase
- 56 participants
- Enrollment target
- 1
- Study location
Study Summary
The addition of dexamethasone to non-liposomal bupivacaine in perineural blocks has been shown to enhance pain control and prolong the time until first request for postoperative narcotics in the fields of orthopedic, thoracic, and gynecologic surgery. This has not been investigated in any types of breast surgery. The investigators assessed if the combination of dexamethasone to bupivacaine in the preoperative field block prior to bilateral breast reduction surgery resulted in improved pain control relative to bupivacaine alone.
Conditions Studied
Interventions
- DRUG Saline
- DRUG Dexamethasone 4mg
Study Locations (1)
Pennsylvania
- Temple University Hospital - Philadelphia
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 56 participants |
| Start Date | 2017-09-29 |
| Est. Completion | 2020-11-25 |
| Phase | Phase 2 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04919317
The ClinicalTrials.gov registry entry for NCT04919317 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 56 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 (79% lower). The listed sponsor is Temple University, which has 163 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Saline is the first listed.
NCT04919317 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.
Frequently Asked Questions
What is clinical trial NCT04919317 about?
NCT04919317 is a clinical study titled "Combination Dexamethasone and Bupivacaine Pain Control in Reduction Mammaplasty". The addition of dexamethasone to non-liposomal bupivacaine in perineural blocks has been shown to enhance pain control and prolong the time until first request for postoperative narcotics in the fields of orthopedic, thoracic, and gynecologic surgery. This has not been investigated in any types of b...
What is the current status of trial NCT04919317?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 56 participants. The study started on 2017-09-29. Estimated completion is 2020-11-25.
What conditions does trial NCT04919317 study?
This clinical trial studies the following conditions: Pain, Postoperative, Mammaplasty.
What interventions are being tested in trial NCT04919317?
The interventions under investigation include: Saline (DRUG), Dexamethasone 4mg (DRUG).
Who is sponsoring clinical trial NCT04919317?
This trial is sponsored by Temple University, which has 163 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04919317 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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