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NCT05824832 · ClinicalTrials.gov registry record · Phase 4
Buprenorphine, Clonidine, and Dexamethasone on Duration of Brachial Plexus Blocks for Upper Extremity Surgery
A Phase 4 study of Pain, Postoperative, sponsored by Loyola University.
- Recruiting
- Registry status
- Phase 4
- Development phase
- 120
- Enrollment target
- 1
- Study location
NCT05824832 is a Phase 4 study of Pain, Postoperative that is actively recruiting participants, run by Loyola University. The registered enrollment target is 120 participants, below the 272-participant average among 108 other Pain, Postoperative trials with a reported enrollment target (56% lower). The trial reports 1 study location across 1 state.
The verdict
NCT05824832, a Phase 4 study of Pain, Postoperative, is actively recruiting participants, sponsored by Loyola University.
- RECRUITING
- Registry status
- Phase 4
- Development phase
- 120 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to learn if there is a difference in morphine requirements in patients after upper extremity surgeries including shoulder arthroscopy. The main question it aims to answer is whether there is a difference between Interscalene brachial plexus blocks with the addition of buprenorphine, dexamethasone, and clonidine and the same block without the adjuvant.
Conditions Studied
Interventions
- DRUG Interscalene block with the addition of buprenorphine, clonidine, dexamethasone
- DRUG Interscalene block with buprenorphine alone
Study Locations (1)
Illinois
- Loyola University Chicago - Maywood
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2023-02-28 |
| Est. Completion | 2026-06-30 |
| Phase | Phase 4 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05824832
The ClinicalTrials.gov registry entry for NCT05824832 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 120 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 (56% lower). The listed sponsor is Loyola University, which has 92 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Pain, Postoperative appearing as the primary indexed condition, and to 2 interventions - of which Interscalene block with the addition of buprenorphine, clonidine, dexamethasone is the first listed.
NCT05824832 reports 1 study location spanning 1 distinct geographic area - top geographies include Illinois.
Frequently Asked Questions
What is clinical trial NCT05824832 about?
NCT05824832 is a clinical study titled "Buprenorphine, Clonidine, and Dexamethasone on Duration of Brachial Plexus Blocks for Upper Extremity Surgery". The goal of this clinical trial is to learn if there is a difference in morphine requirements in patients after upper extremity surgeries including shoulder arthroscopy. The main question it aims to answer is whether there is a difference between Interscalene brachial plexus blocks with the addition...
What is the current status of trial NCT05824832?
This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 120 participants. The study started on 2023-02-28. Estimated completion is 2026-06-30.
What conditions does trial NCT05824832 study?
This clinical trial studies the following conditions: Pain, Postoperative.
What interventions are being tested in trial NCT05824832?
The interventions under investigation include: Interscalene block with the addition of buprenorphine, clonidine, dexamethasone (DRUG), Interscalene block with buprenorphine alone (DRUG).
Who is sponsoring clinical trial NCT05824832?
This trial is sponsored by Loyola University, which has 92 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05824832 being conducted?
This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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