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To study the effect of two regional anesthesia techniques for adequate pain control after surgeries around hip joint

Comparison of analgesic efficacy of supra-Inguinal fascia iliaca compartment block (S-FICB) and pericapsular nerve group (PENG) block in patients undergoing hip surgery: A prospective randomized controlled study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036787
Enrollment
58
Registered
2021-09-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: M169- Osteoarthritis of hip, unspecified

Interventions

Intervention1: Pericapsular Nerve Group Block: Ultrasound guided deposition of 20 mL bupivacaine 0.5% with epinephrine 5 mcg/mL between psoas tendon and pubic ramus. Control Intervention1: Supra-ingui

Sponsors

AIIMS Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Belonging to American Society of Anesthesiologists Physical Status 1-3 and Scheduled for elective unilateral total hip replacement surgery.

Exclusion criteria

Exclusion criteria: 1. Known hypersensitivity to any of the drugs used in the study. 2. Patient having infection at the site of block. 3. Patients with coagulopathy or on anticoagulation therapy. 4. Patients with untreated psychiatric illness. 5. Patients with known cardiac, hepatic or kidney diseases. 6. Opioid Dependency 7. Pre-existing neurologic or anatomic deficits in the lower extremities 8. Prior surgery in the corresponding side of the inguinal or suprainguinal area 9. Chronic pain syndromes requiring opioid intake at home 10. Pregnancy

Design outcomes

Primary

MeasureTime frame
Post-operative pain relief assessed by Numeric Rating Scale (NRS) at fixed time intervalTimepoint: First 24 postoperative hours

Secondary

MeasureTime frame
1. Motor Blockade at fixed time interval 2. The time of first rescue analgesic requirement. 3. Total amount of analgesia consumed during 24-hours. 4. Duration to perform block. 5. Patient’s satisfaction for the mode of analgesia. 6. Periprocedural complication. Timepoint: First 24 postoperative hours

Countries

India

Contacts

Public ContactSubham Das

All India Institute of Medical Sciences, Jodhpur

drmsadik@gmail.com9414849733

Outcome results

None listed

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