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Regional Block clinical trials

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NCT ID: NCT06231355 Recruiting - Analgesia Clinical Trials

Liposomal vs. Conventional Bupivacaine for Pain Control

Start date: February 21, 2024
Phase: Phase 4
Study type: Interventional

The goal of this pilot study is to test the hypothesis that liposomal bupivacaine extends the duration of paravertebral block in patients undergoing radical nephrectomy, achieving improved analgesia compared to conventional bupivacaine. The main questions it aims to answer are: - Area under curve of numeric rating scale of pain from 12 to 72 h after surgery. - Cumulative opioid consumption during the period of 12 to 72 h after surgery.

NCT ID: NCT05652075 Recruiting - Post Operative Pain Clinical Trials

PENG and LFCN Block Versus Lumbar Plexus Block for Postoperative Analgesia After Total Hip Arthroplasty

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

Regional anesthesia for postoperative analgesia in THA includes epidural anesthesia and peripheral nerve blocks. However epidural anesthesia has a great role in THA, it has become restricted as perioperative antithrombotic drugs are generally used for orthopedic patients. the study aim to evaluate and compare efficacy and safety of pericapsular nerve group block (PENG) block and lateral femoral cutaneous nerve versus Lumbar plexus block on postoperative analgesia in hip surgery.

NCT ID: NCT05633329 Completed - Post Operative Pain Clinical Trials

Dual Injection ESPB Versus Single Injection ESPB for Laparotomies

Start date: December 7, 2022
Phase: N/A
Study type: Interventional

To evaluate and compare the efficacy of single level injection erector spinae plane block versus double level injection Erector spinae plane block in laparotomies

NCT ID: NCT04773730 Completed - Regional Block Clinical Trials

Quadratus Lumborum Block Type 2 Versus Posterior Transversus Abdominus Plane Block

quadratus
Start date: March 15, 2021
Phase: N/A
Study type: Interventional

This patient population are at risk of adverse effects secondary to inadequate pain management such as inadequate maternal bonding and late ambulation. Regional analgesia is preferred due to their opioid sparing effects and reduction in related adverse effects but the analgesia from these blocks is not known which one is superior to the other in the context of cesarean section

NCT ID: NCT04371705 Completed - Postoperative Pain Clinical Trials

Efficacy of Ultrasound Guided Erector Spinae Plane Block

Start date: October 15, 2018
Phase: N/A
Study type: Interventional

Thoracic epidural and paravertebral blocks are the most widely regional technique used for postoperative analgesia after surgery, but they are difficult to perform and carry a risk of serious complication. In this study, investigator asses the efficacy of ultrasound ESPB on intraoperative and postoperative hemodynamics and patient satisfaction

NCT ID: NCT03777592 Recruiting - Pain, Postoperative Clinical Trials

Perioperative Erector Spinae Plane Block in Thoracoscopic Surgery

Start date: December 15, 2018
Phase: N/A
Study type: Interventional

The erector spinae plane block (ESPB) is a novel myofascial plane block. The ESPB is targeted at anterior surface of the erector spinae plane, which is oriented cephalocaudally to the spinal transverse process. Local anaesthetic injected in this plane can block the dorsal rami and ventral rami and intercostal nerves. The aim of this study was to evaluate the effect of ESPB on postoperative pain in thoracic surgery.

NCT ID: NCT01473667 Terminated - Pain Clinical Trials

Superficial Cervical Plexus Block for Pacemaker Insertion

Start date: November 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate clinical outcomes from two current standard of care pain control procedures performed for patients undergoing pacemaker insertion.