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NCT05095909 · ClinicalTrials.gov registry record · NA
Utility of Intermittent Cryo-Compression Versus Traditional Icing Following Arthroscopic Rotator Cuff Repair
A NA study of Rotator Cuff Injuries and Cryotherapy Effect, sponsored by Allina Health System.
- Recruiting
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT05095909 is a NA study of Rotator Cuff Injuries and Cryotherapy Effect that is actively recruiting participants, run by Allina Health System. The registered enrollment target is 100 participants, above the 91-participant average among 10 other Rotator Cuff Injuries trials with a reported enrollment target (10% higher). The trial reports 1 study location across 1 state.
The verdict
NCT05095909, a NA study of Rotator Cuff Injuries and Cryotherapy Effect, is actively recruiting participants, sponsored by Allina Health System.
- RECRUITING
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
Effective post - operative pain control following orthopedic surgical procedures without excessive reliance upon opioid pain medication has garnered increased attention in recent years. This study will evaluate the utilization of a non-invasive, novel cryo - compression, post-operative modality to improve pain control versus standard ice wraps in the immediate post-operative phase of arthroscopic rotator cuff surgery via a randomized controlled study design. Furthermore, if this study demonstrates improved pain control, improved quality of life and decreased opioid usage with the intermittent cold compression unit, recommendations may be considered for system-wide utilization.
Conditions Studied
Interventions
- DEVICE Cryo-compression
- OTHER Cryo-therapy
Study Locations (1)
Minnesota
- Allina Health Orthopedics - Plymouth
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2024-08-05 |
| Est. Completion | 2026-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05095909
The ClinicalTrials.gov registry entry for NCT05095909 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 100 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 91-participant average among 10 other Rotator Cuff Injuries trials with a reported enrollment target (10% higher). The listed sponsor is Allina Health System, which has 32 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Rotator Cuff Injuries appearing as the primary indexed condition, and to 2 interventions - of which Cryo-compression is the first listed.
NCT05095909 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.
Frequently Asked Questions
What is clinical trial NCT05095909 about?
NCT05095909 is a clinical study titled "Utility of Intermittent Cryo-Compression Versus Traditional Icing Following Arthroscopic Rotator Cuff Repair". Effective post - operative pain control following orthopedic surgical procedures without excessive reliance upon opioid pain medication has garnered increased attention in recent years. This study will evaluate the utilization of a non-invasive, novel cryo - compression, post-operative modality to i...
What is the current status of trial NCT05095909?
This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2024-08-05. Estimated completion is 2026-12.
What conditions does trial NCT05095909 study?
This clinical trial studies the following conditions: Rotator Cuff Injuries, Cryotherapy Effect.
What interventions are being tested in trial NCT05095909?
The interventions under investigation include: Cryo-compression (DEVICE), Cryo-therapy (OTHER).
Who is sponsoring clinical trial NCT05095909?
This trial is sponsored by Allina Health System, which has 32 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05095909 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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