Comparison of the Impacts of Ultrasound-guided Pericapsular Nerve Group (PENG) Block Applied in Different Volumes on Postoperative Pain in Hip Replacement Surgeries: A Randomized Clinical Trial

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Postoperative pain management has an important place in anesthesia practices. In order to ensure patient comfort after the surgery, to start postoperative rehabilitation early, and to prevent the process from causing mood disorders such as anxiety and pathological conditions such as chronic pain syndrome, the pain caused by the operation in the postoperative period must be effectively relieved. Pericapsular nerve group (PENG) block; It is a regional anesthesia technique that targets the anterior capsule of the hip joint and aims to block the joint branches of the accessory obturator nerve and femoral nerve by administering local anesthetic. Although it has been described recently, controlled prospective studies in the literature have shown it to be a safe and effective regional technique for postoperative pain after hip surgery. However, volume studies on this block are limited. Therefore, in this study, we aimed to determine the optimal dose by comparing the effectiveness of PENG block on pain using different local anesthetic volumes.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: t
View:

• Patients with informed consent

• Patients planned for hip surgery

• Those between the ages of 18-80

• ASA (American Society of Anesthesiologists) I-III patients

Locations
Other Locations
Turkey
Istanbul Medeniyet University
RECRUITING
Istanbul
Contact Information
Primary
Gokce Alis, MD
alisgokce@gmail.com
+905368265875
Backup
Mesure Gul Nihan Ozden, MD
nihanozdenn@gmail.com
+905323614400
Time Frame
Start Date: 2023-06-20
Estimated Completion Date: 2023-12-20
Participants
Target number of participants: 50
Treatments
Active_comparator: Group 1
PENG block was planned to be applied to group 1 patients with 20 cc of 0.25% bupivacaine.
Active_comparator: Group 2
PENG block was planned to be applied to group 2 patients with 10 cc of 0.25% bupivacaine.
Related Therapeutic Areas
Sponsors
Leads: Istanbul Medeniyet University

This content was sourced from clinicaltrials.gov