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NCT05215236 · ClinicalTrials.gov registry record · NA
Opiate Sparing Protocol Randomized Controlled Trial in Open Distal Radius Fracture Repair
A NA study of Distal Radius Fracture, sponsored by Campbell Clinic.
- Completed
- Registry status
- NA
- Development phase
- 72
- Enrollment target
- 1
- Study location
NCT05215236: Completed NA study of Distal Radius Fracture, sponsored by Campbell Clinic.
NCT05215236 is a NA study of Distal Radius Fracture that has completed, run by Campbell Clinic. The registered enrollment target is 72 participants, below the 246-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (71% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05215236, a NA study of Distal Radius Fracture, has completed, sponsored by Campbell Clinic.
- COMPLETED
- Registry status
- NA
- Development phase
- 72 participants
- Enrollment target
- 1
- Study location
Study Summary
A comparison of oral morphine equivalents between an opiate sparing cohort and an opiate based cohort following open reduction internal fixation of a distal radius fracture.
Primary Outcome
opiate pill count
Conditions Studied
Interventions
- OTHER Opiate Sparing
- OTHER Opiate Based
Study Locations (1)
Tennessee
- Campbell Clinic - Germantown
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 72 participants |
| Start Date | 2022-03-01 |
| Est. Completion | 2025-06-30 |
| Phase | NA |
What the finished NCT05215236 record still lists
NCT05215236 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 72 participants, a relatively small participant target, below the 246-participant average among 11 other Distal Radius Fracture trials with a reported enrollment target (71% lower).
The record links to 1 condition, with Distal Radius Fracture appearing as the primary indexed condition, and to 2 interventions - of which Opiate Sparing is the first listed.
NCT05215236 reports a single indexed study location in Tennessee.
Frequently Asked Questions
What is clinical trial NCT05215236 about?
NCT05215236 is a clinical study titled "Opiate Sparing Protocol Randomized Controlled Trial in Open Distal Radius Fracture Repair". A comparison of oral morphine equivalents between an opiate sparing cohort and an opiate based cohort following open reduction internal fixation of a distal radius fracture.
What is the current status of trial NCT05215236?
This trial is currently completed. It is a NA study. The enrollment target is 72 participants. The study started on 2022-03-01. Estimated completion is 2025-06-30.
What conditions does trial NCT05215236 study?
This clinical trial studies the following conditions: Distal Radius Fracture.
What interventions are being tested in trial NCT05215236?
The interventions under investigation include: Opiate Sparing (OTHER), Opiate Based (OTHER).
Who is sponsoring clinical trial NCT05215236?
This trial is sponsored by Campbell Clinic, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05215236 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Distal Radius Fracture
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 NCT05215236's enrollment target sits among peer trials
72 8th of 11 higher than 4 of 11 other Distal Radius Fracture trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Distal Radius Fracture 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
-
Hematoma Block for Distal Radius Fracture
RECRUITING · NA
-
Quantitative and Clinical Assessment of Flexor Tendon Gliding Following Application of a Bioresorbable Hydrogel: A Prospective, Randomized Study in Patients Undergoing Distal Radius Fracture Repair
RECRUITING · NA
-
Postoperative Immobilization and Physical Therapy Following Volar Locked Plating for Distal Radius Fractures
ACTIVE NOT RECRUITING · NA
-
Utility of Cortical Bone Tissue Properties in the Assessment of Fracture Risk
ACTIVE NOT RECRUITING · NA
-
Perioperative Glucocorticoid Administration in the Treatment of Adult Distal Radius Fractures
RECRUITING · Phase 4
-
Impact of Early ADL Participation on Outcomes Post DRF
RECRUITING · Phase 1
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