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Anesthesia, Local clinical trials

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NCT ID: NCT04453462 Completed - Clinical trials for Carpal Tunnel Syndrome

Efficacy of Local Direct Median Nerve Block

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

Carpal tunnel syndrome is the most common compressive neuropathy. Carpal tunnel release is indicated when failed conservative treatment. Although it can be done either with local anesthesia or brachial plexus block, there is no gold standard of anesthetic choice. The study is conducted to compare the efficacy of two methods and we hypothesized that the local direct median nerve block has effectiveness in intraoperative pain control not inferior to brachial plexus block in endoscopic carpal tunnel release.

NCT ID: NCT04452656 Completed - Analgesia Clinical Trials

Analgesic Efficacy of Ultrasound Guided Bilateral Erector Spinae Plane Block in Pediatric.

Start date: July 20, 2020
Phase: N/A
Study type: Interventional

This randomized, double-blinded, study aims to compare the efficacy of analgesia and any side effects of U/S guided bilateral Erector SpinaePlane block versus non-block t paediatric patients undergoing corrective cardiac surgeries.

NCT ID: NCT04445636 Completed - Anesthesia, Local Clinical Trials

Efficacy of Dexmedetomidine Versus Morphine as an Adjunct to Bupivacaine in Caudal Anesthesia.

Start date: June 28, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to compare the duration of postoperative analgesia, and any side effects of caudal dexmedetomidine versus morphine in combination with bupivacaine in pediatric patients undergoing thoracic surgeries.

NCT ID: NCT04444635 Completed - Anesthesia, Local Clinical Trials

Serratus Anterior Plane Block in Pediatric Patients

Start date: June 14, 2020
Phase: N/A
Study type: Interventional

The aim of this work is to study the efficacy of ultrasound guided serratus anterior plane block in pediatric patients undergoing thoracic surgeries. It is a randomized controlled trial.

NCT ID: NCT04395690 Completed - Anesthesia, Local Clinical Trials

Comparing Two Anesthetic Techniques for Implant Placement

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

To evaluate in a comparative way the patient's perception in implant surgery in the posterior mandibular quadrants depending on whether the operation is performed under trunk anaesthesia or infiltrative anaesthesia, in both cases with Articaine. Randomized and multicenter prospective study to be developed in eight centers with similar socio-professional characteristics, with the same operative protocol. A significant sample of patients will be randomized to undergo the same intervention (surgery to place implants in the posterior mandible) under one or another type of anesthesia (inferior alveolar block nerve or infiltrative) and data will be collected using a Numerical Rate scale on four occasions (after the incision, after drilling, after suturing and after 12h).

NCT ID: NCT04356521 Completed - Anesthesia, Local Clinical Trials

Lateral Sagittal vs Costoclavicular Approach for Ultrasound-Guided Infraclavicular Block

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

An ultrasound-guided infraclavicular block performed with the costoclavicular (CC) approach and the lateral sagittal (LS) approach will be compared in patients scheduled for forearm and hand surgery.

NCT ID: NCT04337060 Completed - Prostate Cancer Clinical Trials

Open Radical Prostatectomy and Erector Spinae Plane Block

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

In the proposed study, a bilateral erector spinae plane (ESP) block [10 ml 1%lidocaine + 10 ml 0.5 % bupivacaine vs normal saline (NS)] will be performed preoperatively to patients undergoing open radical prostatectomy. Analgesic efficacy will be assessed on the numeric rating scale (NRS) along with intra- and 24 h post-operative narcotic consumption.

NCT ID: NCT04298099 Completed - Anesthesia, Local Clinical Trials

Ropivacaine Plasma Concentrations and Pharmacokinetics Following Erector Spinae Plane Block in the Pediatric Population

Start date: December 18, 2020
Phase: Phase 4
Study type: Interventional

The primary aim of this study is to evaluate the pharmacokinetics of serum ropivacaine concentrations following erector spinae plane peripheral nerve blocks in the pediatric population. Secondary outcomes will assess the efficacy of the block with perioperative morphine equivalent consumption and pain scores.

NCT ID: NCT04222010 Completed - Pain, Postoperative Clinical Trials

Serratus Plain Block Versus Paravertebral Block Versus Serratus Plain Block and Paravertebral Block for Postoperative Pain Following Thoracoscopic Surgery

thoracoscopic
Start date: January 2, 2020
Phase: N/A
Study type: Interventional

Acute and chronic postoperative pain remains a major concern following thoracoscopic surgery. Firstly because pain constitutes a serious concern for patients after surgery, and secondarily because an ineffective control of pain may lead to postoperative morbidity, especially in lung cancer surgery. To date, several procedures have been described but the best modality of locoregional analgesia for thoracoscopic surgery has not been assessed yet. The main objective of this study is to evaluate efficiency of several validated approaches for preoperative locoregional analgesia, comparing serratus plain block versus paravertebral block versus serratus plain block and paravertebral block for postoperative pain following thoracoscopic surgery. To this end, the investigators will conduct an interventional prospective monocentric, double blind, compared and randomized study. Previously to thoracoscopic surgery, patients will be randomized in one of the three following arms: serratus plain block, paravertebral block or serratus plain block and paravertebral block combined.

NCT ID: NCT04205773 Completed - Anesthesia, Local Clinical Trials

Epidural Catheter Location by Epidural Pressure Waveform

Start date: November 1, 2019
Phase:
Study type: Observational

The aim of this preliminary study was to evaluate the new CompuFlo instrument which allows pulsatile waveform recordings.