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NCT06321718

Pericapsular Nerve Group Block vs Supra Inguinal Fascia Iliaca Compartment Block

Comparison Between Pericapsular Nerve Group (PENG) Block With Lateral Femoral Cutaneous Nerve Block and Supra Inguinal Fascia Iliaca Compartment Block (S FICB) for Traumatic Hip Fixation Surgeries: a Randomized Controlled Trial
Assiut University·ClinicalTrials.gov·procedureNot yet recruiting
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Study focus
Disease/Condition
Pain, Postoperative
Drug/Device/Intervention
PENG + LFCN block versus S-FICB
Study type
Interventional
Intervention type
procedure
Sponsor & location
Primary sponsor
Assiut University
Timeline & enrollment
Phase
N/A
Start date
May 01, 2024
End date
Apr 01, 2025
Enrollment
96 participants
Primary outcome

recording time for return of full muscle power

Summary

This study aims to assess the efficacy of PENG block performed with LFCN block in controlling
 postoperative pain and promoting motor function recovery and to compare its effectiveness
 with S-FICB.

ICD-10 classifications
During surgical operationDuring surgical operationDuring surgical operationPain, unspecifiedPostoperative intestinal obstruction
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06321718
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06321718 through Pure Global AI's free database. This phase not specified trial is sponsored by Assiut University and is currently Not yet recruiting. The study focuses on Pain, Postoperative. Target enrollment is 96 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.