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Comparison of Ultrasound-guided fascia iliaca compartment block with bupivacaine and intravenous morphine sulphate in proximal femoral fracture geriatrics patients in Emergency Department

Comparison of Ultrasound-guided fascia iliaca compartment block with bupivacaine and intravenous morphine sulphate in proximal femoral fracture geriatrics patients in Emergency Department

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20221227002
Enrollment
26
Registered
2022-12-27
Start date
2022-02-24
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Ultrasound-guided fascia iliaca compartment block (US-FICB) intravenous (IV) morphine older adults hip fracture pain in the emergency department (ED). Hip fracture, Ultrasound-guided fascia iliaca compartment block, older adult

Interventions

0.5% bupivacaine 20 ml in NSS 10 ml (maximum dose 2mg/kg) according to the randomization list. Patient was in supine position. Subjects in US-FICB group inguinal area was disinfected and draped, steri
Experimental Drug,Active Comparator Drug
Ultrasound-guided fascia iliaca compartment block (US-FICB) , intravenous (IV) morphine

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
60 Years to 120 Years

Inclusion criteria

Inclusion criteria: 1. patients aged 60 and above who presented to the ED from February 2022 to November 2022 with diagnosis of isolated hip fracture including neck of femur, intertrochanter and subtrochanteric area. 2. Pain score of 5 or above from visual analog scale (VAS).

Exclusion criteria

Exclusion criteria: 1.hemodynamic instability (defined as systolic blood pressure <90 or >180 mmHg, heart rate <50 or >150 beats/min, or respiratory rate <10 or >30 breaths/min) 2.allergic to morphine and local anesthesia 3.skin infection at injection site 4.creatine clearance < 50 ml/min 5.opioid use within 4 hours 6.communication deficits 7.body weight <40 kg or >115 kg 8.need immediate surgical intervention 9.traumatic brain injury 10previous bypass surgery of affected limb

Design outcomes

Primary

MeasureTime frame
pain score 15,30,60 mins visual analog scale

Secondary

MeasureTime frame
adverse events 15,30,60 mins questionaire report

Countries

Thailand

Contacts

Public Contactwasinee chanpichai

Faculty of Medicine Vajira Hospital Navamindradhiraj University

wasinee@nmu.ac.th0841111790

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026