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Does the nerve block around hip joint capsule reduce pain in patients with proximal femur fractures

Role of Pericapsular Nerve Group (PENG) Block in attenuating pain in the patients with proximal femur fractures - a randomized control trial - NA

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/055277
Enrollment
50
Registered
2023-07-17
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Pericapsular Nerve Group Block: Block is to be given around hip joint capsule in patients with proximal femur fractures including neck of neck, intertronchanteric, subtronchanteric and

Sponsors

Indira Gandhi Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients will be considered for the study if they have a suspected proximal femur fracture. To be eligible for the inclusion, a proximal femur fracture, including intracapsular or extracapsular, had to be confirmed on either radiograph or computed tomography (CT) reported by a radiologist, who belong to ASA I, II, and III categories who are more than 18 years of age will be enrolled.

Exclusion criteria

Exclusion criteria: Patients who refuse to participate in the study. Patients with known allergy to local anesthetics. Patients with a history of coagulopathy or on anticoagulant and antiplatelet drugs. Patients with infection at the site of block. Poly trauma patients. Patients who cannot assess pain reliably (dementia).

Design outcomes

Primary

MeasureTime frame
To compare PENG block analgesia with the control group (traditional pain management methods) in cases of proximal femur fractures in emergency.Timepoint: 24 hours

Secondary

MeasureTime frame
To calculate the duration of action of PENG block analgesiaTimepoint: 24- 36 hours;To compare the requirement for rescue analgesia in both groupsTimepoint: 24 hours;To compare patient satisfaction & any side effects occurring in both groupsTimepoint: 24 hours

Countries

India

Contacts

Public ContactDr Preetika

Department of Anesthesia, IGMC Shimla

shwetamahajan437@gmail.com9418040187

Outcome results

None listed

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