Viewing Study NCT06183528



Ignite Creation Date: 2024-05-06 @ 7:55 PM
Last Modification Date: 2024-10-26 @ 3:16 PM
Study NCT ID: NCT06183528
Status: RECRUITING
Last Update Posted: 2024-06-27
First Post: 2023-11-30

Brief Title: Effects of Pericapsular Nerve Group Block on Postoperative Recovery for Total Hip Arthroplasty
Sponsor: Umraniye Education and Research Hospital
Organization: Umraniye Education and Research Hospital

Study Overview

Official Title: Effects of Pericapsular Nerve Group Block on Postoperative Recovery for Total Hip Arthroplasty
Status: RECRUITING
Status Verified Date: 2024-10
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The hypothesis of this study is that patients who undergo PENG block in before Total Hip Artroplasthy THA surgery with spinal anesthesia will have reduced postoperative pain scores less need for opioid analgesics and earlier mobilisation
Detailed Description: This prospective randomised controlled study included a total of 60 patients aged 40-85 years who underwent THA surgery under spinal anaesthesia Patients were divided into two groups as PENG block n30 and non-PENG block n30 PENG block was placed in the fascial plane between the pseudotendon and pubic ramus with USG in-plane technique 20 ml of 05 bupivacaine was administered and surgery was initiated The primary outcome of the study was to investigate the effect of preoperative PENG block application on postoperative pain opioid requirement mobilisation time hip joint patency and length of hospital stay in patients undergoing THA surgery The secondary outcome was to investigate the effect of PENG block on perioperative haemodynamics and postoperative side effects

For multimodal analgesia 10 ml 05 bupivacaine 10 ml 2 lidocaine is infiltrated into the surgical wound incision line by the surgical team at the end of surgery After tramadol 50 mg loading with PCA device a basal rate of 5-10 mghour 20 mg bolus dose 30 minutes lock time is given with paracetamol 10 mgkg iv 8 hours interval

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None