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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02804542
Enrollment
29
Registered
2016-06-17
Start date
2016-08-11
Completion date
2019-05-31
Last updated
2023-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hip Fracture

Keywords

fascia iliaca blocks

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.

Interventions

OTHERObservational

Sponsors

Grand Rapids Medical Education Partners
CollaboratorOTHER
Corewell Health West
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* low energy femoral neck and pertrochanteric-type hip fractures * age 65+ * 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

Design outcomes

Primary

MeasureTime frameDescription
Total Pre-op IV Morphine Equivalents (TIVME)From Date of admission until date of surgery, approximately 48 hoursIV morphine equivalent dosing pre-operatively

Secondary

MeasureTime frameDescription
Mean Pre-op Pain ScoreFrom Date of admission until date of surgery, approximately 48 hoursMean patient-reported pain score
Length of Hospital Stay (LOS)Through study completion, approximately 5 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026