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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 is a NA study that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 68 participants.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04925791
The ClinicalTrials.gov registry entry for NCT04925791 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 68 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which standardized pre-conditioning treatment is the first listed.
NCT04925791 reports 0 study locations.
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.
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