Preoperative Analgesia: The Effectiveness of the PENG Block in Patients With Hip Fractures

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-95
SponsorSakarya University

About this trial

The aim is to provide effective preoperative analgesia in patients undergoing surgical procedures due to hip fractures by administering a pericapsular nerve group (PENG) block under ultrasound guidance. This approach seeks to increase patient satisfaction, reduce analgesic requirements, enable earlier discharge, and decrease morbidity and mortality.

Eligibility criteria

Qualifiers

Patients undergoing hip farcture surgery

Disqualifiers

Chronic analgesics consumption

Patients contraindicated for neuraxial anesthesia

Alcohol and drug addiction

Allergies to local anesthetics and opioids

Trial design

Treatments tested in this trial

  • PENG block with 0.25% bupivacaine guided by ultrasound.

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators