The advantage of combining two nerve blocks to decrease the post operative pain in hip fracture surgeries.

Analgesic efficacy of combining pericapsular nerve group block (PENG) with lateral femoral cutaneous nerve block (LFCN) in fractured hip surgeries under spinal anaesthesia - a randomised double blind trial. - Nil

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/06/068790

Enrollment

Registered

2024-06-12

Start date

Unknown

Completion date

Unknown

Last updated

2024-06-24

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

Conditions

Health Condition 1: - Health Condition 2: O- Medical and Surgical

Interventions

Intervention1: Ultrasound guided Pericapsular Nerve Group Block: USG guided Pericapsular Nerve Group Block with 25 ml of 0.25% of Ropivacaine + 4 mg dexamethasone Duration of procedure: 15 minutes Con

Eligibility

Inclusion criteria

Inclusion criteria: All willing and consenting participants, American Society of Anaesthesiologist (ASA) physical status I-III

Exclusion criteria

Exclusion criteria: Participants with coagulopathy , cardiovascular disease , psychiatric illness, speech and hearing impairment, morbidly obese and those allergic to anaesthetic drugs

Design outcomes

Primary

Measure	Time frame
The time required to request for the 1st rescue analgesia with tramadol in minutes.Timepoint: at 0 minutes , 30 minutes , 60 minutes, 90 minutes	—

Secondary

Measure	Time frame
Any complications or adverse effect would be measured.Timepoint: 24 HOURS;Ease of spinal Positioning score assessed using a four-point scale.Timepoint: 30 MINUTES;Patient satisfaction score.Timepoint: 24 hours;The Numerical Rating Scale (NRS) for Pain recorded post block at rest and upon movement i.e. by passively lifting the limb 15° above the resting level.Timepoint: 30 minutes;Total tramadol consumption.Timepoint: 24 HOURS	—

Measure

Time frame

Any complications or adverse effect would be measured.Timepoint: 24 HOURS;Ease of spinal Positioning score assessed using a four-point scale.Timepoint: 30 MINUTES;Patient satisfaction score.Timepoint: 24 hours;The Numerical Rating Scale (NRS) for Pain recorded post block at rest and upon movement i.e. by passively lifting the limb 15° above the resting level.Timepoint: 30 minutes;Total tramadol consumption.Timepoint: 24 HOURS

—

Countries

India

Contacts

Public ContactUjjaini Ray

Kalinga Institute of Medical Sciences

meet.laxmans1@gmail.com9958538812

Outcome results

None listed

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