Efficacy of Pericapsular Nerve Group (PENG) Block for Hip Surgeries - Trial NCT06144931
Access comprehensive clinical trial information for NCT06144931 through Pure Global AI's free database. This phase not specified trial is sponsored by Suez Canal University and is currently Recruiting. The study focuses on Pain, Postoperative. Target enrollment is 38 participants.
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Study Focus
Sponsor & Location
Suez Canal University
Timeline & Enrollment
N/A
Jun 01, 2023
Mar 01, 2024
Primary Outcome
The time of first request of analgesia in both groups
Summary
To study the efficacy of the PENG block on the duration of postoperative analgesia. There are
 two groups of patients, who are undergoing hip joint surgeries, one group (Control Group)
 will receive spinal anesthesia only while the other group (PENG Group) will receive PENG
 block before spinal anesthesia.
ICD-10 Classifications
Data Source
ClinicalTrials.gov
NCT06144931
Non-Device Trial