A trial to compare the effectiveness of two different dose of a drug bupivacaine (0.125% and0.25%) in US guided PENG block ease of positioning for regional anaesthesia( spinal )for hip surgery patients

Evaluation of two different doses of bupivacaine (0.25% and 0.125%)20ml in US guided pericapsular nerve group block for ease of positioning for spinal anaesthesia during hip surgery - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/03/064128

Enrollment

Registered

2024-03-14

Start date

Unknown

Completion date

Unknown

Last updated

2024-04-01

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: PENG block: 20ml of bupivacaine (0.125% or 0.25% ) given 30min before spinal anaesthesia under US guidance and comparison of drug effect in ease of positioning for spinal anaesthesia af

Eligibility

Inclusion criteria

Inclusion criteria: Patient scheduled for hip surgeries under subarachnoid block who are American Society of Anaesthesiologist (ASA) physical status I -III and consenting

Exclusion criteria

Exclusion criteria: 1.Fractures older than 2 weeks 2.Patients who were unwilling 3.Patients having no pain while sitting 4.Any bleeding disorder and patient on anticoagulants 5.Neurological and musculoskeletal disease 6.Local infection at the injection site 7.History of allergy to local anaesthetic and signs of allergy to lignocaine test dose

Design outcomes

Primary

Measure	Time frame
compare ease of positioning for spinal anaesthesia with 0.125% and 0.25% bupivacaine in US guided PENG block within 30 min of administrationTimepoint: 30 minutes after Us guided PENG block	—

Secondary

Measure	Time frame
Haemodynamic monitors at rest and 15 degrees leg elevation at 0,10 and 20,30 minutes after giving US guided PENG blockTimepoint: 3yrs;Time to rescue analgesia in the two groups will be notedTimepoint: 3yrs;To analyse pain using visual analogue scale at rest and 15 degrees passive leg elevation at 0,10 and 20,30 minutes after giving US guided PENG blockTimepoint: 3yrs	—

Countries

India

Contacts

Public ContactDr Athira E M

Dr Rajendra Prasad government Medical College

shelkbj@yahoo.com

Outcome results

None listed

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