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Clinical Trials/NCT02804542
NCT02804542
Completed
Not Applicable

Pre-operative Fascia Iliaca Blocks and Opioid Requirements in Hip Fracture Patients

Spectrum Health Hospitals0 sites29 target enrollmentAugust 11, 2016
ConditionsHip Fracture

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fracture
Sponsor
Spectrum Health Hospitals
Enrollment
29
Primary Endpoint
Total Pre-op IV Morphine Equivalents (TIVME)
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to determine if non-continuous local anesthetic fascia iliaca blocks performed in the emergency department are effective for preoperative analgesia in hip fracture patients. Investigators hypothesize that patients with these blocks will have lower opioid requirements than patients in a historical group in whom blocks were not performed.

Registry
clinicaltrials.gov
Start Date
August 11, 2016
End Date
May 2019
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • low energy femoral neck and pertrochanteric-type hip fractures
  • intact cognition upon admission and ability to provide written informed consent

Exclusion Criteria

  • pathologic fractures (tumor)
  • high energy fractures
  • concomitant fractures besides hip fractures
  • chronic home opioid exposure prior to hospitalization
  • moderate to severe dementia
  • pre-fracture hospitalization
  • time from arrival to block \>6 hours
  • time from arrival to OR \<6 hours or \>48 hours

Outcomes

Primary Outcomes

Total Pre-op IV Morphine Equivalents (TIVME)

Time Frame: From Date of admission until date of surgery, approximately 48 hours

IV morphine equivalent dosing pre-operatively

Secondary Outcomes

  • Mean Pre-op Pain Score(From Date of admission until date of surgery, approximately 48 hours)
  • Length of Hospital Stay (LOS)(Through study completion, approximately 5 days)

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