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Anesthesia, Local clinical trials

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NCT ID: NCT04472299 Recruiting - Anesthesia, Local Clinical Trials

Paravertebral Block to Reduce the Incidence of New Onset Atrial Fibrillation After Cardiac Surgery

Start date: April 9, 2021
Phase: Phase 4
Study type: Interventional

The purpose if this pilot study is to determine if a perioperative infusion of 0.2% ropivacaine via bilateral T3 paravertebral catheters can decrease the incidence of new onset atrial fibrillation following primary CABG and/or valve surgery and compare a number of secondary outcomes.

NCT ID: NCT04458467 Completed - Pain, Acute Clinical Trials

Perineural Local Anesthetic Administration With a Continuous Infusion Versus Automatic Intermittent Boluses

Start date: July 15, 2020
Phase: N/A
Study type: Interventional

This will be a randomized comparison of continuous local anesthetic infusion with patient controlled boluses (PCA) to automated boluses with PCA for continuous popliteal sciatic nerve blocks. The goal will be to determine the relationship between method of local anesthetic administration (continuous with PCA initiated at discharge vs. intermittent dosing with PCA with a 5-hour delay) for continuous peripheral nerve block and the resulting pain control and duration of analgesia.

NCT ID: NCT04458142 Not yet recruiting - Anesthesia, Local Clinical Trials

Efficiency of Single Buccal Infiltration Versus Buccal and Intrapapillary Infiltration

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

Everyday practice in dentistry is based on giving the painless injection and achieving adequate local anesthesia. Various techniques of reducing injection pain in children can be broadly categorized as psychological and physical. The psychological approach includes behavior management techniques, physical means and other recent techniques such as computer controlled anesthesia, electronic dental anesthesia, and so forth. However, none of these techniques have been successful in eliminating pain, fear and anxiety in children. Direct palatal injection technique is difficult to administer without significant pain or discomfort since there is little tissue space at these sites between the mucosa and the underlying periosteum. Studies conducted on indirect palatal injection technique (intrapapillary) revealed that it reduces the pain of palatal injection with the same efficacy of anesthesia during extraction. The desirable method to evade pain during palatal injection is just not to have one. Maxillary molars removal without palatal or multiple injections is possible due to relatively thin porous bone of posterior buccal maxilla that facilitates the diffusion of local anesthetic.

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: NCT04440475 Recruiting - Pain, Postoperative Clinical Trials

Tap Block vs Conventional Pain Medication for Patients Undergoing Robotic Sacrocolpopexy

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

The purpose of this study is to assess whether the transversus abdominis plane block (Tap block) is different than the oral postoperative pain medications in controlling pain after robotic sacrocolpopexy.

NCT ID: NCT04427904 Recruiting - Postoperative Pain Clinical Trials

Bupivacaine Versus Lidocaine Infiltration for Postoperative Pain in Thyroid Surgery

Start date: June 1, 2022
Phase: Phase 2
Study type: Interventional

The purpose of this study is to compare the efficacy of Bupivicaine and Lidocaine for postoperative pain control in thyroid surgery.

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).