Effects of Pericapsular Nerve Group (PENG) Block Applied for Analgesia on the Postoperative Process in Patients Undergoing Hip Fracture Surgery.

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In this study, it was aimed to compare the multimodal analgesia application or the pericapsular nerve group (PENG) block methods in patients undergoing hip surgery. The effectiveness and benefit rate of the PENG block in postoperative pain will be evaluated. Postoperative pain, need for additional analgesia, range of motion of the hip joint, mobilization time, length of hospital time and adverse events in patients undergoing hip fracture surgery with and without PENG block will be investigated.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 30
Maximum Age: 85
Healthy Volunteers: f
View:

• Patients who will undergo hip fracture surgery Women and men aged 30-85

Locations
Other Locations
Turkey
Umraniye Education and Research Hospital
RECRUITING
Istanbul
UmraniyeERH
RECRUITING
Istanbul
Contact Information
Primary
Zeliha Tuncel, MD
zelihalara@yahoo.com
+905053577483
Backup
Hale Arkan Tuna, MD
halearkan@yahoo.com.tr
+905303705619
Time Frame
Start Date: 2023-11-21
Estimated Completion Date: 2025-07-30
Participants
Target number of participants: 70
Treatments
Active_comparator: PENG Block group
PENG block group; USG probe is placed on the transverse plane medial to the anterior inferior iliac spine (AIIS), the medial end of the probe is placed on the superior pubic It is rotated approximately 45° counterclockwise to align it with the ramus. For the PENG block, an 80 mm block needle is placed in the fascial plane between the psoas tendon and pubic ramus and 20 ml of 0.5% bupivacaine is administered after spinal anesthesia,
Other: Control group
Control group; 10 ml 0.5% bupivacaine + 10 ml 2% lidocaine is infiltrated into the surgical area by the surgical team at the end of surgery
Related Therapeutic Areas
Sponsors
Leads: Umraniye Education and Research Hospital

This content was sourced from clinicaltrials.gov