CompletedNot Applicable

Effect of PENG Block on Postoperative Tramadol Consumption in Partial Hip Prosthesis Surgery

Turkey (Türkiye)48 participantsStarted 2022-03-01

Plain-language summary

This study aims to evaluate the effect of ultrasound-guided pericapsular nerve group (PENG) block on postoperative tramadol consumption, pain scores, and clinical outcomes in patients undergoing partial hip prosthesis surgery. Patients aged 18-75 years scheduled for surgery under general anesthesia were divided into two groups: those receiving PENG block and those not receiving the block. Postoperative tramadol consumption within the first 24 hours, visual analog scale (VAS) and numeric rating scale (NRS) scores, hemodynamic parameters, additional analgesic requirements, and recovery characteristics were recorded and compared between groups. The findings of this study are expected to contribute to optimizing multimodal analgesia strategies in hip surgery.

Who can participate

Age range18 Years – 75 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Patients aged between 18 and 75 years * Patients scheduled for partial hip prosthesis surgery * Patients classified as ASA physical status I-III * Patients who provided written informed consent Exclusion Criteria: * Known allergy to local anesthetics * Coagulation disorders or anticoagulant therapy contraindicating regional anesthesia * Infection at the injection site * Severe systemic disease (ASA IV or higher) * Cognitive impairment preventing reliable pain assessment * Refusal to participate in the study

What they're measuring

Total Tramadol Consumption Within 24 Hours After Surgery

Timeframe: 24 hours postoperatively

Trial details

NCT IDNCT07534137

SponsorUniversity of Gaziantep

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2022-10-01

View on ClinicalTrials.gov More Hip Fracture trials