Fascia Iliaca Compartment Block For Analgesia After Total Hip Arthroplasty
Completed · Not applicable · Has a placebo group
Conditions studied: Pain Disorder, Sensory Deficit
In brief
Introduction Fascia Iliaca compartment block (FICB) is commonly used to treat pain in patients after total hip arthroplasty (THA) despite the lack of RCTs to evaluate the efficacy of FICB for this indication. Therefore the objective of this study was to assess the analgesic benefit of FICB for post-operative pain management in THA. Methods After IRB approval and informed consent, patients having THA at our center in the period 2010-2011 were recruited. Eligible patients were adults, ASA physical status I-III, and BMI \<30) with no contraindication to study procedures. In the PACU, all patients received morphine sulfate IVPCA; patients reporting pain \> 3 on the NRS-11 despite IVPCA were randomized by the method of sealed envelopes to receive US guided injections of 30ml 0.5% ropivacaine (FICB) or 30ml 0.9% NaCl (sham block, SB) beneath the fascia iliaca. The primary outcome variable was opioid analgesic consumption during the first 24 h postoperatively. Secondary outcome measures were pain intensity (NRS-11) and extent of sensory blockade.
Key facts
- Study ID
- NCT01758497
- Run by
- St. Luke's-Roosevelt Hospital Center
- People needed
- 32
- Starts
- 2010-10-01
- Expected to finish
- 2011-08-01
- Last updated by the study team
- 2016-12-29
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Adults
- ASA physical status I-III
- BMI<30
- No contraindications to study procedures
You may not qualify if…
- Pediatric patients
- ASA physical status IV
- BMI>30
- Contraindications to study procedures
- Hypersensitivity to local anesthetics
Where it is running
- St Luke's Roosevelt Hospitals — New York, New York, United States
Full record on ClinicalTrials.gov
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