Local Infiltration Analgesia for Hip Arthroscopy
Not Applicable
Completed
- Conditions
- Pain
- Registration Number
- NCT01454518
- Lead Sponsor
- Trinity Health Of New England
- Brief Summary
The purpose of this study is to examine if ultrasound guided infiltration of local anesthetic solution around the hip joint will provide effective pain control after hip arthroscopy.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 36
Inclusion Criteria
- hip arthroscopy
- ages 18-80
Exclusion Criteria
- history of neurological disease
- diabetes
- pregnancy
- neuropathy
- chronic narcotic use
- allergy to local anesthetic solution
- inability to give consent or cooperate with the study protocol
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Post operative opioid consumption. Within 24 hours after surgery Amount in milligrams of opioid consumption post surgery in the recovery room and for a 24 hour period.
- Secondary Outcome Measures
Name Time Method Pain scores in recovery room. Within 24 hours of the surgery Mesures of pain score using numeric pain rating scale (0=no pain, 10=worst pain) completed by patient in recovery room and every 6 hours for a 24 hour period after discharge from recovery room.
Trial Locations
- Locations (1)
Saint Francis Hospital and Medical Center
🇺🇸Hartford, Connecticut, United States
Saint Francis Hospital and Medical Center🇺🇸Hartford, Connecticut, United States