MedPath

PENG VERSUS FIB

Not Applicable
Recruiting
Conditions
Pain with total hip arthroplasty due to osteoarthritis.
Osteoarthritis of hip
Registration Number
IRCT20230809059091N2
Lead Sponsor
CMH Rahim Yar Khan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
150
Inclusion Criteria

Included all ASA-II (American society of Anaesthesiologists) male and female patients above the age of fifty years
Requiring total hip arthroplasty (THA) due to advanced osteoarthritis of the hip joint.

Exclusion Criteria

Excluded patients with major cardiac or respiratory debility, metastatic bone disease, allergy to drugs used for the block, bleeding diathesis, coagulation defects, patients with patchy or failed block after administration and patients not willing to be included in the study.
Metastatic bone disease
Allergy to the drugs used in the block (lignocaine)
Bleeding diathesis and coagulation disorders
Patients with patchy or failed block after administration
Patients not willing to be included in the study

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Mean time for first dose of rescue analgesia and mean time to patient mobilization. Timepoint: Within 12 hours post-surgery. Method of measurement: Standard Visual Analog scale for pain assessment.
Secondary Outcome Measures
NameTimeMethod
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