Hip Dislocation, Hip Fractures, Hip Injuries
Conditions
Brief 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.
Detailed description
Subjects will be asked to take part in one of two treatment procedures 24 hours prior to their scheduled hip arthroscopy date. Subjects will be randomized into either the IPC or CON group. These treatments consist of either 3 rounds of 5 minutes of occlusion alternating with 5 minutes of reperfusion or 3 rounds of 5 minutes of minimal occlusion alternating with 5 minutes of reperfusion. The treatment will last 30 minutes. Days 0-7 post-op will consist of self-reported pain scales and opioid consumption documentation in the morning and evening. This is a randomized single-blind research study. This study has two study groups: * The IPC group will get a standardized pre-conditioning treatment 24 hours prior to their hip arthroscopy. This consists of 3 rounds of 5 minutes of occlusion alternating with 5 minutes of reperfusion while seated. * The CON group will get a controlled treatment of 20% of limb occlusion pressure 24 hours prior to their hip arthroscopy. This consists of 3 rounds of 5 minutes of minimal occlusion alternating with 5 minutes of reperfusion while seated.
Interventions
DIAGNOSTIC_TESTstandardized pre-conditioning treatment
3 rounds of 5 minutes of full occlusion alternating with 5 minutes of reperfusion while seated.
DIAGNOSTIC_TESTPartial occlusion
3 rounds of 5 minutes of partial occlusion alternating with 5 minutes of reperfusion while seated.
Sponsors
Cedars-Sinai Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Patients undergoing a primary hip arthroscopy by the PI between the ages of 18 and 55.
Exclusion criteria
* Patients younger than 18 or older than 55 who have had a previous hip arthroscopy, venous thromboembolism, and/or who take medications and/or supplements known to increase the risk of blood clots.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain levels VAS score | 7 days post op | Pain score 0-10 with 0 being no pain and 10 being the worst |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| number of days opioids were consumed post op | 7 days post op | Total number days the patient had to take pain medication |
Countries
United States
Outcome results
None listed