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Comparative study between two block technique that helps in pain management of hip fracture patients

COMPARISON BETWEEN PERICAPSULAR NERVE GROUP BLOCK AND FASCIA ILIACA BLOCK FOR POSITIONING IN HIP FRACTURE PATIENTS BEFORE NEURAXIAL BLOCKâ?? A RANDOMIZED CONTROLLED PILOT STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029247
Enrollment
40
Registered
2020-11-19
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: S720- Fracture of head and neck of femur

Interventions

Intervention1: FASCIA ILIACA COMPARTMENT BLOCK: Fascia iliaca compartment block with 20ml 0.25% ropivacaine before positioning for neuraxial block in hip fracture patients Intervention2: PERICAPSULAR

Sponsors

ALL INDIA ISTITUTE OF MEDICAL SCIENCES NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with age above 18 years, undergoing surgery for hip fracture under neuraxial block.

Exclusion criteria

Exclusion criteria: Patient refusal. Any contraindication to neuraxial block like coagulopathy, local infection, increased ICP, spine trauma etc. Known allergy to local anaesthetic drugs. Peripheral neuropathy. Hemodynamically unstable polytrauma patients. Patients who are ASA 4 and above.

Design outcomes

Primary

MeasureTime frame
To assess and compare the analgesic efficacy of USG guided pericapsular nerve group (PENG) block with fascia iliaca compartment block (FICB) using VAS score during positioning of hip fracture patients within 30 minutes before neuraxial block.Timepoint: At 10, 20, 30 minutes—

Secondary

MeasureTime frame
To compare the patientâ??s acceptance of the technique.Timepoint: At 24 hour;To compare the postoperative 24-hour analgesic requirement in the two groups. Timepoint: 24 hour;To compare the quality of positioning in the two groups for neuraxial block which will be assessed by the anaesthesiologistâ??s satisfaction and spinal angle.Timepoint: At 30 minute;To study any complications associated with the block.Timepoint: 24 hour monitoring—

Countries

India

Contacts

Public ContactSARINA K

ALL INDIA INSTITUTE OF MEDICAL SCIENCES, NEW DELHI

drchhavisawhney@gmail.com9818357051

Outcome results

None listed

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