Clinical Trials Logo

Anesthesia, Local clinical trials

View clinical trials related to Anesthesia, Local.

Filter by:

NCT ID: NCT02957903 Completed - Pain, Postoperative Clinical Trials

Sensory Distribution of Lateral Femoral Cutaneous Nerve Block

Start date: November 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate and describe the anatomical distribution of the sensory outcome following LFCN block (LFCN = lateral femoral cutaneous nerve) in relation to the incisional lines after Total Hip Arthroplasty (THA). Furthermore, is the aim to examine whether there is a motorial outcome corresponding to the Femoral nerve. The trial will be conducted in healthy volunteers in a blinded, randomized paired study.

NCT ID: NCT02718976 Completed - Pain, Postoperative Clinical Trials

Shamrock - Ultrasound/MR Image Fusion Guided Lumbar Plexus Block

Start date: March 2016
Phase: Phase 2
Study type: Interventional

The main objective is to complete a double-blinded randomized controlled crossover trial of lumbar plexus block with the Shamrock technique guided by ultrasound (US)/magnetic resonance imaging (MRI) image fusion vs. the Shamrock technique guided by ultrasound in healthy volunteers. The investigators will assess block procedure-related parameters, anatomical spread of local anesthetic, and motor and sensory effects.

NCT ID: NCT02713685 Completed - Anesthesia Local Clinical Trials

Comparison of Combined Sciatic(Winnie's) Femoral Nerve Block, and Subarachnoid Block Anesthesia for Lower Limb Surgery

Start date: June 2015
Phase: N/A
Study type: Interventional

60 ASA grades- I, II or III patients, undergoing lower limb surgeries, will be randomly allocated in 2 groups of 30 patients each. In group S- subarachnoid block with 0.5% Bupivacaine (hyperbaric) 2.5ml will be given in lateral position and group B received femoral 3 in 1 block in supine position(with landmark technique) with 20 ml of 0.25% of Bupivacaine, followed by Sciatic block in lateral position with 20 ml of 0.25% Bupivacaine. Onset and duration of sensory and motor block, time of first analgesic requirement, VAS Scores at end of block and surgery, hemodynamic effects, patients' and surgeon's satisfaction will be evaluated.

NCT ID: NCT02626559 Completed - Anesthesia, Local Clinical Trials

Serum Bupivacaine Concentration Levels After Injection of Liposomal Bupivacaine Into the Knee

Start date: November 2015
Phase: N/A
Study type: Observational

Serum levels of bupivacaine over time after peri-articular injection of a mixture of liposomal bupivacaine and plain bupivacaine during total knee arthroplasty.

NCT ID: NCT02593370 Completed - Hip Fractures Clinical Trials

Suprasacral Parallel Shift - Ultrasound/MR Image Fusion Guided Lumbosacral Plexus Block

Start date: October 2015
Phase: Phase 1
Study type: Interventional

The main objective of the trial is to complete a double-blinded randomized controlled trial with crossover design of a lumbosacral plexus block with the Suprasacral Parallel Shift technique guided by ultrasound/magnetic resonance (MR) image fusion vs. Suprasacral Parallel Shift guided by ultrasound by estimating sensory block of the femoral nerve, the obturator nerve, the lumbosacral trunk, and spinal nerve L1 in healthy volunteers.

NCT ID: NCT02255591 Completed - Pain, Postoperative Clinical Trials

Shamrock Versus Lumbar Ultrasound Trident - Ultrasound Guided Block of the Lumbar Plexus

Start date: February 2015
Phase: Phase 4
Study type: Interventional

The main objective of the trial is to complete a double-blinded randomized controlled trial of a lumbar plexus block with the Shamrock technique versus the Lumbar Ultrasound Trident technique by estimating the time of performance of lumbar plexus blocks in healthy volunteers. Secondary objectives include a) estimates of number and depth of needle injections, distance of injection site from the midline, minimal electric nerve stimulation to trigger muscular response and the type of response, and volunteer discomfort during block injection, b) measurements of plasma lidocaine and mean arterial blood pressure, c) examinations of sensory block of the dermatomes T8-S3 and motor block of the femoral nerve, the obturator nerve, the hip abductor muscles, and the hamstring muscles, d) success rate of lumbar plexus block, e) perineural and epidural distribution of local anesthetics added contrast visualized on magnetic resonance imaging (MRI) scanning, and f) cost-effectiveness for the Shamrock technique versus the Lumbar Ultrasound Trident Technique for lumbar plexus block in healthy volunteers. The hypothesis is that the Shamrock technique is faster to perform than the Lumbar Ultrasound technique, and that the success rate of the Shamrock technique is equal to or higher than the Lumbar Ultrasound Trident technique.

NCT ID: NCT01751256 Completed - Postoperative Pain Clinical Trials

Additional Effect of Wound Infiltration After Cesarean Section With Optimal Standard Analgesia

KTcesar
Start date: June 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine wether wound infiltration brings additional analgesia effect after cesarean section with optimal standard postoperative analgesia

NCT ID: NCT01679392 Completed - Anesthesia, Local Clinical Trials

A Study Investigating Properties of the Transversus Abdominis Plane Block

Start date: August 2012
Phase: N/A
Study type: Interventional

In this study we investigate the following properties of the transversus abdominis plane block in healthy volunteers: 1. Cutaneous analgesic distribution 2. Muscular affection 3. Reproducibility

NCT ID: NCT01474382 Completed - Anesthesia, Local Clinical Trials

Study of OraVerse® for Safety and Efficacy in Pediatric Dental Patients

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether OraVerse is safe and effective for the reversal of dental anesthesia in children 2 to 5 years of age weighing at least 10 kg.

NCT ID: NCT01418690 Completed - Anesthesia, Local Clinical Trials

Changes in Tissue Oxygenation Following Regional Anesthesia

Start date: September 2011
Phase: N/A
Study type: Observational

Adequate tissue oxygenation is required for effective white blood cell function and bactericidal activity. Decreased tissue oxygenation is a risk factor for perioperative wound infections. Regional anesthetic techniques result in a functional sympathetic block and may increase tissue oxygenation. The purpose of this study is to evaluate changes in tissue oxygenation using a non-invasive Near-infrared spectroscopy (NIRS) device. The current study will evaluate changes in tissue oxygenation following regional anesthetic techniques (peripheral nerve blockade and neuraxial techniques such as caudal block) in pediatric patients). Regional anesthesia will induce a sympathetic blockade and improve tissue oxygenation.