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Comparative study of conventional based vs ultrasound guided pericapsular nerve group block(PENG) for positional comfort during spinal or epidural anesthesia in patients with fracture femur

Comparative study of nerve stimulator based vs USG guided pericapsular nerve group block(PENG) for positional comfort during central neuraxial block in patients with fracture femur

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/02/049418
Enrollment
86
Registered
2023-02-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Interventions

Intervention1: USG guided PENG block for positional comfort during central neuraxial block using 0.75% ropivacaine: Comparative study of nerve stimulator based vs USG guided pericapsular nerve group(P

Sponsors

vijayanagar institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: a)Patients of 50-80 years of age, of either sex, posted for elective/emergency hip surgeries under central neuraxial block b)ASA physical status 1 and 2 c)Patient with normal cardiopulmonary function

Exclusion criteria

Exclusion criteria: a)Refusal by patients for procedure b)Patients with deranged coagulation profile or with bleeding diathesis c)Patient with mental ,neurological disorder, severe cardiovascular disease d)Patient with puncture site infection e)History of allergy to local anaesthetic f)Neuromuscular diseases g)History of epilepsy and alcoholism

Design outcomes

Primary

MeasureTime frame
Assessment of reduction in NRS pain scores after administration of PENG BLOCKTimepoint: at baseline and 30 minutes

Secondary

MeasureTime frame
1) onset ,duration and quality of blockade 2) side effects if any like local hematoma formation , vascular puncture, signs of any local anaesthetic toxicity will be noted Timepoint: at baseline and 30 minutes

Countries

India

Contacts

Public ContactSRINIVASALU D

Vijayanagar institute of medical sciences

suhas9887@gamil.com7676353003

Outcome results

None listed

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