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Analgesic Efficacy of USG Guided Pericapsular Nerve Group Block Versus Intravenous Nalbuphine Hydrochloride In Patients of bony hip injuries: A Randomised Control Trial

Analgesic Efficacy of USG Guided Pericapsular Nerve Group Block Versus Intravenous Nalbuphine Hydrochloride In Patients of Intracapsular And Pericapsular Bony Hip Injuries: A Randomised Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/04/032715
Enrollment
60
Registered
2021-04-09
Start date
Unknown
Completion date
Unknown
Last updated
2022-11-21

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 (PENG): Patients undergoing PENG block with injection bupivacaine 0.25% 25 ml. Control Intervention1: Intravenous Nalbuphine Hydrochloride: Patients under

Sponsors

Aiims Bhubaneswar
Lead Sponsor
Dr Upendra Hansdah
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: patients presenting with traumatic injuries to the hip and radiologically confirmed to be a 1. fracture of surgical neck of the femur 2. intertrochanteric fracture of femur 3. sub capital fracture of the femur 4. fracture of acetabulum 5. fracture of the pubic ramus 6. patients with NRS pain score>=5

Exclusion criteria

Exclusion criteria: 1. Infection over the skin at the site of block 2. The shaft of femur fracture 3. Allergic to local anesthetic 4. Coagulopathy 5. Pregnancy 6. Altered mental status 7. Hip Dislocation 8. patient not giving consent 9. patients who received analgesic before the block 10. Associated with other bony injuries(except the inclusion criteria).

Design outcomes

Primary

MeasureTime frame
Numerical rating scale (NRS Scale)Timepoint: Numerical rating scale (NRS Scale)baseline,30 mins,1 hour,2 hour,4 hour,6 hour—

Secondary

MeasureTime frame
To determine the need for rescue analgesia in both arms.Timepoint: 6 hours,12 hours;To study the adverse effect in both the arms.Timepoint: 30 mins,2 hours,4 hours, 6hours, 12 hours—

Countries

India

Contacts

Public ContactDr Nishit Kumar Sahoo

AIIMS Bhubaneswar

drsangeeta.asth@gmail.com2472312

Outcome results

None listed

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