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NCT01378949 Clinical Trial

Psoas Compartment Block Versus Fascia Iliaca Block After Total Hip Arthroplasty

Pain Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01378949
Other study ID # 2259-11-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 19, 2011
Last updated June 22, 2011
Start date September 2011
Est. completion date September 2013

Study information
Verified date June 2011
Source Hillel Yaffe Medical Center
Contact Anatoly Stav, MD
Phone 972-4-630-4529
Email stav@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial 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.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 90
Est. completion date September 2013
Est. primary completion date September 2013
Accepts healthy volunteers No
Gender Both
Age group 45 Years to 90 Years
Eligibility 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)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• Bupivacaine
Bupivacaine 0.5% with adrenaline 5 mcg/cc
• Morphine
Morphine 1 mg/cc

Locations
Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)
Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain score of patients who have been given FICB for post-operative pain relief after THA 3 days No
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