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Comparison of Analgesic Efficacy of PENB Block with FICB in Post Operative Hip Fracture Patients

Comparison of Analgesic Efficacy of Ultrasound Guided Pericapsular Nerve Group Block Versus Fascia Iliaca Compartment Block in Patients of Hip Fracture

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05810012
Enrollment
50
Registered
2023-04-12
Start date
2022-04-01
Completion date
2022-10-31
Last updated
2025-02-12

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

Conditions

Hip Fracture Surgery, Post-operative Pain Management

Brief summary

This study was done to evaluate two different interventions for postoperative pain control in patients undergoing hip surgeries. Fifty patients, divided in two equal groups, were included in the study. Patients in Group P were given pericapsular nerve group (PENG) block while those in Group F were given fascia iliaca compartment block (FICB). Pain score, using Numeric Rating scale as a measurement tool, was assessed at one, six, eighteen and twenty fours after the procedure as a primary outcome. Total tramadol consumption in milligrams was recorded as a secondary outcome.

Interventions

DRUGPENG block

10ml of 0.125% isobaric bupivacaine injected

20ml of 0.125% isobaric bupivacaine injected

Sponsors

Pain Medicine Department
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* surgical correction of fracture neck of femur under spinal anaesthesia

Exclusion criteria

* allergy to local anaesthetics * bleeding disorders * morbid obesity with BMI more than 35 * patients of chronic pain * drug addiction * psychiatric issues

Design outcomes

Primary

MeasureTime frameDescription
Pain score using Numeric Rating scale24 hoursPain scored assessed after completion of surgery at one, six, eighteen and twenty fours

Secondary

MeasureTime frameDescription
Total Tramadol consumption24 hoursTotal Tramadol consumption In twenty four hours

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026