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Pericapsular nerve group block (an innovative nerve block) is beneficial for patients with hip fracture undergoing surgery for perioperative pain relief

Study of effectiveness of Pre induction USG guided pericapsular nerve group(PENG) block in minimizing pain associated with positioning for neuraxial anesthesia in patients with hip fractures: A prospective randomized control study - not applicable

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084207
Enrollment
32
Registered
2025-04-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Health Condition 1: S720- Fracture of head and neck of femur Health Condition 2: S721- Pertrochanteric fracture

Interventions

Intervention1: Group P: Pericapsular Nerve Group Block with Ropivacaine 0.25 percent 20ml for perioperative pain relief Control Intervention1: Group C: Control group will receive a intravenous dose 1

Sponsors

Jaipur Golden Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients consenting for the intervention (PENG block) and regional anesthesia 2. Age 20 years to 90 years of either gender 3. ASA grade1,2 or 3

Exclusion criteria

Exclusion criteria: 1. Patients refusal for regional anesthesia and if any contraindication is present. 2. Any strong contraindication for opioid analgesics like advanced chronic lung disease with respiratory failure, severe OSA etc 3. Allergy to any drug under study. 4. Patients with coagulopathy or on anticoagulants. 5. Patients with evidence of Cardiac failure. 6. Any infection at the site of block 7. Patient unable to communicate

Design outcomes

Primary

MeasureTime frame
To measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution and NPRS scoringTimepoint: Baseline, 30mins—

Secondary

MeasureTime frame
To observe numerical pain rating scale (NPRS) score, before and after intervention (PENG block/IV opioid) and during positioning for spinal anaesthesia and compare the outcome of the cases with that of control groupTimepoint: Perioperative;To measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution.Timepoint: Perioperative;To study whether preoperative PENG block has any influence on post operative analgesia by noting time for first demand of analgesia after completion of surgeryTimepoint: 24-48 hours;To observe the hemodynamic changes from baseline till execution of neuraxial block in both the study and the control group and compareTimepoint: Perioperative—

Countries

India

Contacts

Public ContactDR BEJOY S GEORGE

Jaipur Golden Hospital

abhijeet72@gmail.com9958995277

Outcome results

None listed

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