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Continuous Fascia Iliaca Compartment Block in Geriatric Hip Fracture

Pain Management in Geriatric Hip Fracture Patients With Ultrasound-guided Continuous Fascia Iliaca Compartment Block

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04914988
Enrollment
20
Registered
2021-06-07
Start date
2018-02-01
Completion date
2019-02-15
Last updated
2021-06-07

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

Conditions

Acute Pain Due to Trauma, Hip Fractures

Brief summary

The patient with hip fracture who has Numerical Rating Scale (NRS) ≥ 5 at rest or on movement will be indicated for USG FICB at Emergency Department or patient's ward. The aim of this prospective observation study was evaluated the efficacy and complications of cFICB in adult hip fracture preoperatively.

Detailed description

The Enhance Recovery Program of pain management in geriatric hip fracture has been set up as a part of fast track at Siriraj Hospital since September 2017. The ultrasound-guided (USG) fascia iliaca compartment block (FICB) is routinely offered to patients with a hip fracture by acute pain service (APS) anesthesiologist. The patient with hip fracture who has Numerical Rating Scale (NRS) ≥ 5 at rest or on movement will be indicated for USG FICB. The aim of this prospective observation study was evaluated the efficacy and complications of cFICB in adult hip fracture preoperatively.

Interventions

None listed

Sponsors

Mahidol University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* patient age equal or more than 65 years old * patient with acute hip fracture within 7 days * patient with NRS ≥ 5

Exclusion criteria

* patient refusal * history of local anesthetic allergy * inability to communicate or cognitive dysfunction * multiple fracture involvement

Design outcomes

Primary

MeasureTime frameDescription
numerical rating scale at restChange from baseline numerical rating scale at 30 minutes post-blocknumerical rating scale 0-10 (0=no pain, 10=worst pain)
numerical rating scale during movementChange from baseline numerical rating scale at 30 minutes post-blocknumerical rating scale 0-10 (0=no pain, 10=worst pain)

Secondary

MeasureTime frameDescription
Numerical rating scale during movementWithin 48 hours postoperativenumerical rating scale 0-10 (0=no pain, 10=worst pain)
Rate of complications of continuous fascia iliaca compartment analgesiaWithin 48 hours postoperativelocal anesthetic systemic toxicity, leakage, infection
Duration of hospital admissionfrom hospital admission until hospital discharge, an average of 1 weeknumber of days
Number of participants with morbidity and mortality6 weeks after hospital dischargemyocardial disease, deep vein thrombosis, delirium, death

Countries

Thailand

Outcome results

None listed

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