Skip to main content
Clinical Trials/NCT01378949
NCT01378949
Unknown
Not Applicable

Psoas Compartment Block Versus Fascia Iliaca Block After Total Hip Arthroplasty

Hillel Yaffe Medical Center1 site in 1 country90 target enrollmentSeptember 2011
ConditionsPain
InterventionsBupivacaineMorphine

Overview

Phase
Not Applicable
Intervention
Bupivacaine
Conditions
Pain
Sponsor
Hillel Yaffe Medical Center
Enrollment
90
Locations
1
Primary Endpoint
Pain score of patients who have been given FICB for post-operative pain relief after THA
Last Updated
14 years ago

Overview

Brief Summary

A psoas compartment block has been used with good results for postoperative pain relief after total hip arthroplasty (THA). However, case reports describing serious complications after the use of this block, have been reported. The fascia iliaca compartment block (FICB) has been shown to be a reliable block for postoperative pain relief for procedures and injuries involving the hip. The investigators have not found any literature that has compared these two blocks. This study will compare the two blocks when used for post-operative pain relief after THA.

Registry
clinicaltrials.gov
Start Date
September 2011
End Date
September 2013
Last Updated
14 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • ASA Class I-III
  • Patients undergoing THA for osteoarthritis

Exclusion Criteria

  • Skin infections adjacent to block site
  • Allergy to local analgesics
  • Patient unable to understand visual analogue scale (VAS)

Arms & Interventions

PsCB Group

Ultrasound-Guided Psoas Compartment Block will be used in patients for pain relief after THA

Intervention: Bupivacaine

FICB Group

Ultrasound-Guided Fascia Iliaca Compartment Block will be used in patients for pain relief after THA

Intervention: Bupivacaine

Patient-Controlled Analgesia

Patient-controlled analgesia will be used for pain relief after THA

Intervention: Morphine

Outcomes

Primary Outcomes

Pain score of patients who have been given FICB for post-operative pain relief after THA

Time Frame: 3 days

Study Sites (1)

Loading locations...

Similar Trials