Clinical Trials Logo

Clinical Trial Summary

Patients were randomly divided into two groups to receive either ultrasound-guided pericapsular nerve group block (PENG group) or fascia iliaca compartment block (FICB group), using 20 ml of 0.2% ropivacaine


Clinical Trial Description

Participants were randomly divided into two groups : group PENG and group FICB, to receive either ultrasound-guided pericapsular nerve group block or fascia iliaca compartment block, using 50 ml of 0.2% ropivacaine. For the FICB, a linear ultrasound probe was placed in the transverse plane and start scanning at the level of the inguinal crease to identify the femoral artery medially and the femoral nerve lateral to the femoral artery. The iliopsoas muscle should be seen overlying fascia iliaca. The block should be performed proximal to the arterial bifurcation. A 50 mm needle was introduced using an in-plane approach to penetrate the fascia iliaca. The hydro dissection separate the fascia iliaca from the iliac muscle, and a total volume of 20 ml of 0.2% ropivacaine was injected in this created space. The PENG bloc is performed with a low frequency curvilinear ultrasound probe, which was initially placed in a transverse plane over the antero inferior iliac spine and the aligned with the pubic ramus by rotating the probe counterclockwise approximately 45 degrees. In this view, it is possible to observe the iliopubic eminence, the iliopsoas muscle tendon, the femoral artery and the pectineus muscle. A 100 mm needle was inserted from lateral to medial in an in-plane approach to place the tip in the musculofascial plane between the psoas tendon anteriorly and the pubic ramus posteriorly. Negative aspiration should be observed before injection of local anaesthetic and a total volume of 20 ml of 0.2% ropivacaine was injected. Spinal anesthesia was performed after 20 minutes. QoR-15 score was assessed before the intervention and 24 hours postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05968014
Study type Interventional
Source University Tunis El Manar
Contact
Status Completed
Phase N/A
Start date February 1, 2022
Completion date July 31, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT04963751 - ERAS in Pediatric & Adolescent Gynecology Preoperative Counseling N/A
Recruiting NCT04072419 - Application of Enhanced Recovery After Surgery for Congenital Esophageal Atresia During Perioperative Period
Recruiting NCT05564819 - Efficacy and Safety of Acetaminophen in Postoperative Pain Management of Infants Phase 1
Recruiting NCT05613439 - The Fast-track Centre for Hip and Knee Replacement Database
Completed NCT04543214 - Outcome of Enhanced Recovery After Surgery (ERAS) Protocols in Patients Undergoing Small Bowel Surgery
Not yet recruiting NCT05576766 - Enhanced Recovery After Surgery (ERAS) Pathway in Patients Undergoing Robot-Assisted Laparoscopic Radical Prostatectomy N/A
Recruiting NCT05081804 - The Effect of Enhanced Recovery After Surgery (ERAS) for Cesarean Section on Neonatal Blood Glucose N/A
Completed NCT04538235 - Analgesic Non Inferiority of the Thoracic Bi-block in Comparison With Thoracic Epidural for VATS.
Not yet recruiting NCT05914090 - The Application of Enhanced Recovery After Surgery (ERAS) for Cardiovascular Surgery in Adult N/A
Recruiting NCT05541640 - Intraoperative Lidocaine Infusion and Surgery-induced Release of Pro-inflammatory Cytokines After Abdominal Surgery N/A
Not yet recruiting NCT05511194 - Safety and Efficacy of ERAS Therapeutic Protocol for Complicated Appendicitis in Children N/A
Recruiting NCT05528484 - Self-reported Outcomes of Patients in ERAS Nursing N/A
Recruiting NCT04596800 - Prehabilitation Plus ERAS Versus ERAS in Gynecologic Oncology: a Randomized Clinical Trial Phase 3
Completed NCT04648644 - Application of ERAS Protocol in Emergency Surgery
Completed NCT02949518 - Enhanced Recovery After Spine Surgery N/A
Active, not recruiting NCT06457100 - Esmolol Versus Lidocaine on the Quality of Postoperative Recovery in Patients Undergoing Functional Endoscopic Sinus Surgery Phase 1/Phase 2
Recruiting NCT06137976 - Surgeon Perception of Gastric Decompression at Time of Gynecologic Laparoscopy N/A
Completed NCT06118593 - Why in Hospital After Wedge Resection
Active, not recruiting NCT06369194 - POWER AUDIT, Postoperative Outcomes Within an Enhanced Recovery After Surgery Protocol
Recruiting NCT04576533 - Patients Undergoing Laparoscopic Colorectal Surgery Walk Out From Operating Room After Surgery ( WOFOR-C1 ) N/A