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Landmark-Based Continuous Pericapsular Nerve Group Block versus Parentral Analgesia for Postoperative Pain Control and Early Mobilization After Hip Fracture Surgery performed under Spinal Anaesthesia

Landmark-Based Continuous Pericapsular Nerve Group Block Versus Parenteral Analgesia for Postoperative Pain Relief and Early Mobilization After Hip Fracture Surgery Under Spinal Anaesthesia: A Prospective Randomized Controlled Study. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110466
Enrollment
100
Registered
2026-05-12
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Health Condition 1: M00-M99- Diseases of the musculoskeletal system and connective tissue Health Condition 2: M00-M99- Diseases of the musculoskeletal system and connective tissue

Interventions

Intervention1: Continuous Pericapsular Nerve Group (PENG) Block using Landmark Technique: landmark-guided pericapsular nerve group (PENG) block following completion of surgery under spinal anaesthesia

Sponsors

Dr. Vithalrao Vikhe Patil Foundations Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Adult patients aged 18 years and above Patients scheduled for surgical management of hip fracture under spinal anaesthesia American Society of Anesthesiologists (ASA) physical status I III Patients providing written informed consent

Exclusion criteria

Exclusion criteria: Patient refusal Known hypersensitivity to local anaesthetics or opioids Infection at the proposed block site Coagulopathy or anticoagulant therapy contraindicating regional block Pre-existing neurological deficits involving the lower limbs Cognitive impairment precluding reliable pain assessment

Design outcomes

Primary

MeasureTime frame
Study outcomes will be presented as comparative analyses of post-operative pain scores, analgesic requirements, time to first mobilization between two groupsTimepoint: 48 hours

Secondary

MeasureTime frame
incidence of adverse effects, patient satisfaction scores, & length of hospital stay between the two groupsTimepoint: 48 hours

Countries

India

Contacts

Public ContactCHETANA SHRIKANT NEHETE

DR. VITTHALRAO VIKHE PATIL MEDICAL COLLEGE AND HOSPITAL

chetana163@gmail.com9082887500

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026