Clinical Trial

PENG Block Plus Local Infiltration Compared to PENG Block Alone in Hip Surgery

Active, Not Recruiting
View on ClinicalTrials.gov →
Record status
This record was last updated December 18, 2024 (before its estimated May 1, 2025 completion). Its status may not reflect the trial's current state.
Summary
Summary: Pain control after hip surgery is quite important for patients' recovery. Many regional techniques are available with the focus on motor sparing block to speed patient recovery. The investigators will compare pericapsular nerve group (PENG) block in addition to local skin infiltration to PENG block alone. The study population will be included for patient traumatic hip surgery. The study population will be divided into group. First group will receive PENG block and local anaesthetics infiltration and second group will receive PENG block. Our primary outcome is to compare numeric rating scale (NRS) between studied groups, and morphine requirements in the first 24 hours as a secondary outcome.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2023-03-06; most recent amendment 2024-12-15.
Status change: Recruiting → Active, Not Recruiting 2024-12-15
Status change: Not Yet Recruiting → Recruiting 2023-08-19
Trial Details
NCT Number NCT05773365
Lead Sponsor Suez Canal University
Conditions Pain, Hip Fractures, Postoperative Pain, Postoperative Analgesia
Enrollment 122 participants
Start Date 2023-07-18
Primary Completion 2025-05-01 (estimated)
Study Completion 2025-07-01 (estimated)
Updated on ClinicalTrials.gov 2024-12-18