Skip to content

A clinical trial to compare the efficacy of Pericapsular Nerve Group (PENG) Block versus Supra-Inguinal Fascia Iliaca (SIFI) Block for post-operative pain relief in hip surgeries.

Comparison of Pericapsular Nerve Group (PENG) Block versus Supra-Inguinal Fascia Iliaca (SIFI) Block for post-operative analgesia in Hip surgeries.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/04/052079
Enrollment
60
Registered
2023-04-27
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-01

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Pericapsular Nerve Group (PENG) Block for postoperative analgesia in Hip surgeries: Patients in group A will receive an ultrasound-guided Pericapsular Nerve Group (PENG) Block with 30ml

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients aged 40-85 years of age 2. ASA Physical status I, II, III 3. Electively scheduled for hip surgeries. 4. Body mass index between 18-35 kg/m2

Exclusion criteria

Exclusion criteria: 1. Known allergy to study drugs 2. Contraindication to neuraxial blockade or peripheral nerve blocks 3. Chronic opioid use 4. Diabetic neuropathy 5. Infection at the site of block

Design outcomes

Primary

MeasureTime frame
For PRIMARY OUTCOME: Postoperative pain will be measured using VAS pain scores at 24 hours at rest in both the groups.Timepoint: The patients will be monitored hourly for the first 4 hours, 2 hourly for the next 4 hours and then every 4 hourly till 24 hours post-operatively.

Secondary

MeasureTime frame
For SECONDARY OUTCOMES: â?¢ functional mobility will be assessed by assessing quadriceps muscle strength by Manual Muscle Testing scale and maximum weight- bearing possible at 24 hours and 48 hours post- operatively. â?¢ time for first rescue analgesia. â?¢ total opioid consumption in first 24 hours. â?¢ overall patient satisfaction for pain management within 24 hours in both the groups. â?¢ surgeonâ??s satisfaction to anaesthesia services for overall pain management post operatively. Timepoint: Functional mobility and weight bearing will be measured at 24 and 48 hours.

Countries

India

Contacts

Public ContactDr Tanusha Saini

Dayanand Medical College and Hospital

tanushasaini01@gmail.com6239510393

Outcome results

None listed

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