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To compare the effect of ultrasound guided Fascia Iliaca Block versus Epidural Block on postoperative outcome in patients undergoing femoral fracture repair

Comparison of the efficacy of postoperative pain relief in ultrasound guided fascia iliaca block versus epidural block on Quality Of Recovery (QOR â?? 15) in patients undergoing femoral surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/02/017670
Enrollment
80
Registered
2019-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: M95-M95- Other disorders of the musculoskeletal system and connective tissue

Interventions

Intervention1: Group â??IIâ?? :Fascia iliaca block: Patient will be given ultrasound guided fascia iliaca block along with spinal Anaesthesia. After completion of surgery, the patient will be shifted

Sponsors

Government Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing femoral fracture repair Patients with age 50 years to 80 years ASA grade I-III patients Patients able to use to Patient Controlled Analgesia(PCA) pump

Exclusion criteria

Exclusion criteria: Patient refusal to participate in study Patients with any other fracture Patients suffering from concurrent comorbidities (cardiovascular, cerebrovascular, liver or renal) ASA IV - V patients Patients with known hypersensitivity to local anaesthetics Patients with bleeding disorders or on anticoagulants Patients with sepsis Patients with cognitive impairment Patients with absolute / relative contra-indications for spinal anaesthesia

Design outcomes

Primary

MeasureTime frame
Primary outcome defined for the study is Quality of recovery QoR-15.Timepoint: Preoperative, postoperative 24 hours and 48 hours—

Secondary

MeasureTime frame
Secondary outcomes for the study are: Time taken to administer the block, Postoperative VAS score on movement and rest, number of patients requiring additional analgesia, total 24 hour opioid consumption, WHO disability assessment schedule, modified frailty score, prevalence of delirium, mortality, morbidity, total hospital stay and side effects of techniques, if any.Timepoint: VAS score both on rest and movement will be noted at T 0 , T 1 (after 4 hour),T 2 (8 hour),T 3 (12 hour),T 4 (24 hour),T 5 (48 hour) and T 6 (72 hour). Postoperative delirium will also be assessed on postoperative day 0,1,2 and 7 Postoperative morbidity survey will be measured postoperatively on postoperative day 1 till time of discharge. On 30 th day, patient will again be assessed for any disability, frailty, morbidity and mortality.—

Countries

India

Contacts

Public ContactDr Sukanya Mitra

Professor,Government Medical College and Hospital

drsmitra12@yahoo.com

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026