Status:
TERMINATED
Fascia Iliaca Block for Post-Operative Pain Control After Total Hip Arthroplasty
Lead Sponsor:
The Christ Hospital
Conditions:
Osteoarthritis of the Hip
Eligibility:
All Genders
18-75 years
Phase:
PHASE4
Brief Summary
This study evaluates post-operative pain management and narcotic consumption in patients receiving a fascia iliaca block with local anesthetic versus patients receiving fascia iliaca block with saline...
Detailed Description
Although many improvements have been made in implant technology and surgical approaches for total hip arthroplasty, management of post-operative pain remains a major clinical issue. Inadequate pain co...
Eligibility Criteria
Inclusion
- anterior approach total hip arthroplasty (THA) for unilateral osteoarthritis
- English-speaking
- age 18 to 75 years
- American Society of Anesthesiologists (ASA) physical status 1 to 3
- BMI \< 40 kg/m2
- Minimum weight of 50 kg.
- No contraindications to study procedures
Exclusion
- Hip revision surgery
- Allergy to local anesthetics
- Allergy to oxycontin
- Allergy to pregabalin
- Allergy to fentanyl
- Allergy to midazolam
- Allergy to hydromorphone
- BMI \> 40 kg/m2
- Chronic pre-operative opioid use
Key Trial Info
Start Date :
June 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2016
Estimated Enrollment :
72 Patients enrolled
Trial Details
Trial ID
NCT02299271
Start Date
June 1 2014
End Date
December 1 2016
Last Update
February 9 2017
Active Locations (1)
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1
The Christ Hospital
Cincinnati, Ohio, United States, 45219