A Randomized Controlled Trial to Evaluate the Impact of Integrated Preoperative Fascia Iliaca Compartment Block (FICB) for Fast-track Surgery in Elderly Hip Fracture

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This prospective randomized controlled study is aimed to determine the advantages of post-admission fascia iliaca compartment block (FICB) in geriatric hip fracture surgery combination with multimodal analgesia compared with no post-admission FICB. The primary outcome is incidence of delirium during hospital admission. Secondary outcomes are incidence of delirium at hospital discharge, pre- and post-operative pain intensity, peri-operative complications, opioid-related side effects, post-operative complications and length of hospital stay, and morbidities and mortality (in-hospital and 30 days).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 65
Maximum Age: 85
Healthy Volunteers: f
View:

• Patients who are aged ≥65 , \<85 years old and diagnose hip fracture in 8 hospitals

• Planed for fast-track hip surgery

• Isolated acute hip fracture

• Pain on admission during movement ≥ 4 (moderate pain)

Locations
Other Locations
Thailand
Faculty of Medicine Siriraj Hospital, Mahidol University
RECRUITING
Bangkok Noi
Contact Information
Primary
Suwimon Tangwiwat, MD
stangwiwat@yahoo.com
66816456167
Time Frame
Start Date: 2023-05
Estimated Completion Date: 2026-03
Participants
Target number of participants: 420
Treatments
Experimental: Post-admission FICB
Post-admission FICB, drug 0.33% bupivacaine 30 ml + Pre-operative FICB 0.33% bupivacaine 30 ml. Peri-operative pain management protocol : paracetamol + opioid.
No_intervention: Only preoperative FICB
No post-admission FICB + Pre-operative FICB 0.33% bupivacaine 30 ml. Peri-operative pain management protocol : paracetamol + opioid.
Related Therapeutic Areas
Sponsors
Collaborators: Ministry of Health, Thailand
Leads: Mahidol University

This content was sourced from clinicaltrials.gov