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Regional Anesthesia Morbidity clinical trials

View clinical trials related to Regional Anesthesia Morbidity.

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NCT ID: NCT03862612 Completed - Clinical trials for Regional Anesthesia Morbidity

Efficacy of SAP Block Versus ESP Block in VATS Surgery

ESPvSAP
Start date: June 5, 2019
Phase: N/A
Study type: Interventional

During VATS (Video assisted thoracic surgery) small incisions are made in the patient's chest through which a camera and instruments are inserted to allow a lung operation to be performed. Often patients experience a substantial amount of pain and difficult recovery after this type of operation. Anaesthesiologists sometimes use "Regional Anaesthesia" to minimise the pain and help patient recovery after the operation. This involves injecting local anaesthesia into the nerves around the chest wall to effectively numb that part of the chest. There is a variety of different locations on the chest wall where the local anaesthetic can be deposited and no study has measured whether one technique is better than the other in terms of improving patients' recovery experience. Our study compares two new techniques for Regional Anaesthesia after this type of surgery. Participants will be randomly assigned (like tossing a coin) to receive either a SAP (Serratus Anterior Plane) or ESP (Erector Spinae Plane) Block. Both techniques are described within last five years, but have never been compared for chest surgery

NCT ID: NCT03845972 Completed - Postoperative Pain Clinical Trials

Effect of Saphenous Nerve and Nerve to Vastus Medialis Block Within Subsartorial Femoral Triangle on Quadriceps Strength

Start date: April 25, 2018
Phase: N/A
Study type: Interventional

This research objective is to compare quadriceps strength by measuring maximal voluntary isometric contraction (MVIC) and risk of fall before and after subsartorial femoral triangle block (SSFTB)

NCT ID: NCT03805958 Not yet recruiting - Ultrasonography Clinical Trials

Ultrasound-guided Combined Spinal-epidural Anesthesia: Pre-procedure Versus Real-time Scan

Start date: November 15, 2019
Phase: N/A
Study type: Interventional

The investigators will compare the success rate, the consumed time, the number of needle passing, the depth and angle of the needle, the anesthetic effect, complications, pain and patient's satisfaction between 'Real-time scan' and 'Pre-procedure scan', when we performing spinal/epidural combined anesthesia.

NCT ID: NCT03744520 Completed - Clinical trials for Regional Anesthesia Morbidity

Sensorial Block Assessment of Erector Spinae Block

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

Ultrasound-guided erector spinae plane blocks are used as postoperative analgesia method for abdominal, chest and hip surgeries. Regional techniques are well-described methods for postoperative analgesia. However, the sensorial dermatomal spread of regional block varies depending on the multiple variables as the level of the block, local analgesic concentration etc. The aim of this study is to observe dermatomal evaluation of sensorial block.

NCT ID: NCT03740815 Completed - Anesthesia Clinical Trials

Feasibility of Serratus Plane Block Associated With Sedation in Axillary Dissection

Start date: September 25, 2018
Phase: N/A
Study type: Interventional

INTRODUCTION: The axillary lymphadenectomy procedure is known to be associated with late postoperative complications, such as chronic pain and changes in shoulder mobility. Recently, several thoracic ultrasound guided interfascial blocks have been described, including serratus plane block. These blocks were associated with reduced postoperative pain scores in breast surgeries but were never evaluated in axillary dissection. The safety and feasibility of performing axillary dissection under local anesthesia and tumescent anesthesia associated with sedation has been demonstrated in case series, although it is not already the standard technique. DISCUSSION: This project aims to investigate the feasibility of the serratus plane block associated with intra-venous sedation in a prospective case series including 15 patients submitted to axillary dissection, by scoring patient and surgeon satisfaction with the technique, pain, quality of life with EORTC QLQ-C30 questionnaire, and quality of recovery with QoR-40 questionnaire in the first 30 postoperative days.

NCT ID: NCT03740399 Recruiting - Clinical trials for Regional Anesthesia Morbidity

Effect of Modified 45-degree Head-up Tilt Position in Cesarean Operation to the Success of Spinal Anesthesia

cesarean
Start date: April 19, 2018
Phase: N/A
Study type: Interventional

The success of the application of spinal block in 3 different application as the sitting position, side decubitus position and 45 degrees head upside side decubitus position will be evaluated.

NCT ID: NCT03666845 Completed - Clinical trials for Regional Anesthesia Morbidity

Plasma Ropivacaine Concentrations After Sciatic Nerve Block in Patients With Chronic Kidney Disease

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

This prospective observational study aimed to examine the pharmacokinetics of ropivacaine in patients with chronic kidney disease after sciatic nerve block. Sciatic nerve block for foot and ankle surgery will be performed using ropivacaine under ultrasound-guidance, and arterial blood test will be taken for total plasma ropivacaine concentration at 2.5, 5, 15, 30, 60 minutes and 2, 6, 24 hours after sciatic nerve block.

NCT ID: NCT03394807 Completed - Pain Clinical Trials

LaGRA Trial in Laparoscopic Cholecystectomy

LaGRA
Start date: October 1, 2016
Phase: Phase 4
Study type: Interventional

This study investigated the effectiveness of a surgeon administered, laparoscopic guided, regional anaesthesia technique.

NCT ID: NCT03375190 Completed - Clinical trials for Regional Anesthesia Morbidity

A Comparison of Peripheral Nerve Catheter Securement Techniques at the Insertion Site in Healthy Volunteers

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

Continuous peripheral nerve block catheters are used for prolonged analgesia, but are often associated with complications such as catheter failure or dislodgement. This is a single center, prospective study to compare peripheral nerve catheter securement techniques at the insertion site in healthy volunteers.

NCT ID: NCT03368833 Terminated - Clinical trials for Regional Anesthesia Morbidity

Caudal Blockade and Electrocardiographic Changes

Start date: December 15, 2017
Phase:
Study type: Observational

Caudal epidural blockade is frequently used as an adjunct to general anesthesia in children for perioperative analgesia. Intravascular injection of local anesthetic is a known complication that can adversely affect the neurological and cardiovascular systems. This study will look at the delayed effects of a caudal epidural block on the electrical activity of the patient's myocardium by trying to characterize the incidence of ECG changes within 60 minutes after the caudal dose is given.