Ultrasound Guided Local Infiltration Analgesia for Hip Arthroscopy
- Conditions
- Hip Injuries
- Interventions
- Registration Number
- NCT01907191
- Lead Sponsor
- Trinity Health Of New England
- Brief Summary
This study is being undertaken to compare the pain control using either bupivacaine versus liposomal bupivacaine. Liposomal bupivacaine can potentially provide pain relief lasting up to 72 hours while regular bupivacaine can provide pain relief up to 12 hours
- Detailed Description
Patients undergoing hip arthroscopy experience moderate to severe postoperative pain. Effective pain control after surgery is an important component in the overall management of these patients. Good pain control encourages early participation in rehabilitation program, increases success of the surgery, and improves patient satisfaction. Typically, postoperative analgesia is provided to these patients either with nerve blocks or opioid medications. Both these methods provide good pain relief but nerve blocks are associated with weakness of lower extremity muscles which interferes with early ambulation and increase the risk of falls while narcotic medications increase the risk of nausea, vomiting, itching, constipation, ileus, urinary retention, sedation and respiratory depression.
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 23
- Patients having hip arthroscopy
- History of neurologic disease, neuropathy, diabetes
- Allergy to local anesthetic solution
- Chronic use of narcotics
- Inability to give consent/cooperate with study
- History of previous hip arthroscopy on the ipsilateral side
- Pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Liposomal bupivacaine liposomal bupivacaine Ultrasound guided injection of liposomal bupivacaine for patients undergoing hip arthroscopy Bupivacaine Bupivacaine Bupivacaine (around the anterior, lateral and medial aspect of hip joint) for patients undergoing hip arthroscopy
- Primary Outcome Measures
Name Time Method Opioid Consumption (Mean Number of 5mg Oxycontin Tablets Consumed) Post Operative Day 1, 2 & 3 Consumption of 5mg Oxycontin tablets will be assessed on Post Operative Days 1, 2 \& 3.
- Secondary Outcome Measures
Name Time Method Pain Scores Post Operative Day 1, 2 & 3 Analysis of pain scores (at rest and ambulation) during hospital stay. Measured on a 10 point pain scale (1 being no pain and 10 being worst pain imaginable)
Trial Locations
- Locations (1)
Saint Francis Hospital and Medical Center
🇺🇸Hartford, Connecticut, United States