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Clinical Trial Summary

To compare the different analgesic protocols for patients receiving total hip arthroplasty(THA). Patients will divided into 3 groups, which are 1. fascia iliaca compartment block with IV-PCA(patient controlled analgesia), 2. femoral nerve and lateral femoral cutaneous nerve block with IV-PCA, 3. IV-PCA only.


Clinical Trial Description

90 patients will be enrolled and randomized to the 3 different groups.

1. Inclusion criteria:

Patient undergoing THA: 20-75 years old, ASA I-III, general anesthesia with intubation, fentanyl IV PCA.

2. Exclusion criteria Alcohol/substance abuse Rheumatoid arthritis Severe coagulation disorder(PLT<80000 or INR > 1.5) Peripheral neuropathy Allergy to opioids or local anesthetics BMI>35

3. The outcome followers are blinded to the intervention provided.

4. Outcome parameters:

1. Opioid consumption of IV PCA in first 24 hrs.

2. NSAID consumption

3. NRS of pain, the timings of follow-up should be: pre-block, 30

mins post-block, 60 mins post-block, 2 hours post-block, 24hours post-block

4. sensory block in FN, Obturator Nerve and LFCN

5. First request of supplemental IV analgesia ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03231319
Study type Interventional
Source Taichung Veterans General Hospital
Contact Tsung-Yung Tang, M.D.
Phone +886975351575
Email b92401096@gmail.com
Status Recruiting
Phase N/A
Start date July 27, 2017
Completion date April 19, 2018

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