Clinical trial

The Efficiency of Preoperative Pericapsular Nerve Group Block Applied With Ultrasound in Patients With Hip Fracture and Its Effect on the Success of Spinal Anesthesia (PENG)

Name
281570
Description
We aimed to investigate the effectiveness of the pericapsular nerve group (PENG) block applied with preoperative ultrasonography (USG) in patients who were operated on under spinal anesthesia due to hip fracture and whether it influences spinal anesthesia success. The files of 100 patients were reviewed observationally, and 60 patients were included in the study. The patients were divided into two groups: Group P (n = 30) comprising patients who underwent PENG block under USG guidance before the start of surgery and the control group (Group C; n = 30) of patients in whom tramadol infusion was started. From the files of the patients, the transition from the bed to the operating table, lateral decubitus position, skin incision, postoperative exit, postoperative 2nd, 4th, 12th, and 24th hour numeric rating scale (NRS) values, spinal anesthesia duration and number of attempts, and perioperative total tramadol consumption were recorded. During the transfer from the patient bed to the operating table and during the lateral decubitus position, postoperative exit and postoperative 2nd, 4th, 8th, 12th, and 24th hour NRS values were found to be significantly lower in Group P. In addition, lower spinal anesthesia time, lower number of spinal anesthesia attempts, and lower perioperative total tramadol consumption were detected in Group P. We found that PENG block applied preoperatively to patients with spinal anesthesia decreased the perioperative pain score, increased the success of spinal anesthesia by facilitating positioning for spinal anesthesia, and decreased the need for postoperative opioids.
Trial arms
Trial start
2021-12-15
Estimated PCD
2022-04-15
Trial end
2022-06-01
Status
Completed
Treatment
Group PENG
Pericapsular Nerve Group Block (PENG)
Arms:
Group PENG (P)
Group C
Tramadol infusion
Arms:
Group Control (C)
Size
60
Primary endpoint
Change in pain score after applying Pericapsular Nerve Group Block (PENG)
30 minutes after applying PENG block
Pericapsular Nerve Group Block (PENG) block facilitates the success of spinal anesthesia
30 minutes after applying PENG block
Eligibility criteria
Inclusion Criteria: * Over 18 years old * American Society of Anesthesiologists' (ASA) I-II-III Exclusion Criteria: * Patients with a history of chronic pain, * Previous hip joint surgery, * Unsuccessful PENG block or spinal anesthesia application, * Missing data in their records * History of bleeding diathesis * Increased intracranial pressure * Severe mitral and/or aortic stenosis * Allergic to the medications used
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'OTHER', 'timePerspective': 'RETROSPECTIVE'}, 'enrollmentInfo': {'count': 60, 'type': 'ACTUAL'}}
Updated at
2024-04-26

1 organization

1 product

3 indications

Product
Group C
Indication
Efficiency
Indication
Block