Pericapsular Nerve Group Block vs Supra Inguinal Fascia Iliaca Compartment Block - Trial NCT06321718
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.
Study Focus
Sponsor & Location
Assiut University
Timeline & Enrollment
N/A
May 01, 2024
Apr 01, 2025
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
Data Source
ClinicalTrials.gov
NCT06321718
Non-Device Trial

