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NCT04925791 · ClinicalTrials.gov registry record · NA
Does Limb Pre-Conditioning Reduce Pain After Hip Arthroscopy
A NA study, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 68
- Enrollment target
NCT04925791: Completed NA study, sponsored by Cedars-Sinai Medical Center.
NCT04925791 is a NA study that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 68 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT04925791, a NA study, has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 68 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if the utilization of Ischemic Pre-Conditioning 24-hours prior to hip arthroscopy decreases patient's post-operative pain and opioid consumption.
Primary Outcome
Pain score 0-10 with 0 being no pain and 10 being the worst
Interventions
- DIAGNOSTIC_TEST standardized pre-conditioning treatment
- DIAGNOSTIC_TEST Partial occlusion
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 68 participants |
| Start Date | 2021-10-18 |
| Est. Completion | 2023-10-20 |
| Phase | NA |
What the finished NCT04925791 record still lists
NCT04925791 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which standardized pre-conditioning treatment is the first listed.
NCT04925791 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT04925791 about?
NCT04925791 is a clinical study titled "Does Limb Pre-Conditioning Reduce Pain After Hip Arthroscopy". The purpose of this study is to determine if the utilization of Ischemic Pre-Conditioning 24-hours prior to hip arthroscopy decreases patient's post-operative pain and opioid consumption.
What is the current status of trial NCT04925791?
This trial is currently completed. It is a NA study. The enrollment target is 68 participants. The study started on 2021-10-18. Estimated completion is 2023-10-20.
What interventions are being tested in trial NCT04925791?
The interventions under investigation include: standardized pre-conditioning treatment (DIAGNOSTIC_TEST), Partial occlusion (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT04925791?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT04925791's enrollment target sits among peer trials
68 1133rd of 2000 higher than 862 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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
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