NCT05652075View on ClinicalTrials.gov

PENG and LFCN Block Versus Lumbar Plexus Block for Postoperative Analgesia After Total Hip Arthroplasty

NARecruitingINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

January 1, 2023

Primary Completion Date

January 1, 2024

Study Completion Date

February 1, 2024

Conditions
Post Operative PainRegional Block
Interventions
PROCEDURE

pericapsular nerve group and lateral femoral cutaneous nerve block

Will undergo pericapsular nerve group block (PENG) combined with lateral femoral cutaneous nerve under ultrasound guided block with 20 mL of 0.25% bupivacaine.

PROCEDURE

lumbar plexus block

Will undergo Lumbar plexus block (LPB) under ultrasound guided block with 20 mL of 0.25 % bupivacaine.

Trial Locations (1)

61511

RECRUITING

Minia University, Minya

All Listed Sponsors
lead

Minia University

OTHER