MedPath

Fascia Iliaca Blocks for Pain Control After Total Hip Arthroplasty

Phase 4
Completed
Conditions
Arthritis of Hip
Interventions
Procedure: Fascia iliaca compartment block
Drug: Placebo
Registration Number
NCT03375112
Lead Sponsor
Henry Ford Health System
Brief Summary

The fascia iliaca compartment block (FICB) is a regional block that anesthetizes the femoral, obturator, and lateral femoral cutaneous nerves around the hip. The purpose of this study is to determine whether FICB can reduce postoperative pain and increase progress with physical therapy after total hip arthroplasty (THA). This randomized, double-blind, clinical trial will randomize patients to receive either a FICB or placebo after THA. The primary outcomes will be pain scores reported by the patient post-operatively.

Detailed Description

The FICB is a regional block that anesthetizes the femoral, obturator, and lateral femoral cutaneous nerves around the hip joint. There have been numerous study assessing it's ability to control pain in the pre and post operative period in patients with hip fractures. However, there is a limited amount of literature on its efficacy after total hip arthroplasty, and no data when a posterior surgical approach to the hip was utilized. Because regional blocks have been shown to decrease pain post operatively after total knee arthroplasty, we hypothesize that the FICB will decrease pain and narcotic use in patients after total hip arthroplasty. This study will aim to recruit 120 patients that will be randomized to receive a FICB or placebo in the recovery room within 30 minutes of leaving the OR. Once the intervention is complete we will collect data on the patients' pain levels, morphine equivalents of narcotic that they used, and how well they worked with physical therapy during their inpatient stay.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
122
Inclusion Criteria
  • Patients over the age of 18
  • Scheduled for total hip arthroplasty at Henry Ford Hospital
  • Epidural anesthesia during surgery
Exclusion Criteria
  • Pregnancy
  • Known intolerance to local anesthetic or narcotics
  • Revision hip surgery

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Fascia Iliaca Compartment BlockFascia iliaca compartment blockA Fascia Iliaca Compartment Block will be administered in the block room.
ControlPlaceboThe patients will be brought back to the block room, prepped, and a blunt needle will be touched to the skin. A band aid will be applied over the site.
Fascia Iliaca Compartment BlockBupivacaineA Fascia Iliaca Compartment Block will be administered in the block room.
Primary Outcome Measures
NameTimeMethod
Averaged Pain ScorePain scores were at 30 minute intervals for the first hour post-operative, hourly for the next 4 hours, 2 hour intervals for the next 12 hours, then at 4 hour intervals until the 48 hour post-operative or discharge. The mean of these scores is reported.

Analog pains scale 0-10. A pain score of 10 represents maximum pain and a pain score of 0 represents no pain.

Morphine Equivalents ConsumedPostoperative inpatient stay, which averages approximately two days.

Total morphine equivalents (consumed at 4-hour time intervals) received in postoperative inpatient stay.

Secondary Outcome Measures
NameTimeMethod
Walking DistancePost operative day one

The distance the patient is able to walk with physical therapy during their first session

Time to Up-and-goPost operative day one

Time to up and go test performed on the first postoperative day. This test is administered by having the patient sit in a chair. When the patient is instructed to start, the stand from the chair, walk to a marker ten feet away from the chair, turn around, return to the chair, and sit back down. The time is measured as the time from when the start command is given to when they are returned to a seated position.

Time to Discharge ReadinessEvery 6 hours after surgery until completion of inpatient stay, an average of two days days after surgery

Time in hours since surgery to when the patient's pain is controlled on oral medications, has cleared physical and occupational therapy, and has no medical issues that require inpatient treatment.

Trial Locations

Locations (1)

Henry Ford Hospital

🇺🇸

Detroit, Michigan, United States

© Copyright 2025. All Rights Reserved by MedPath