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Anesthesia, Conduction clinical trials

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NCT ID: NCT03369392 Completed - Postoperative Pain Clinical Trials

PANDA-Regional Feasibility Study of a Smartphone Pain Management Application

Start date: December 11, 2017
Phase: N/A
Study type: Interventional

Despite the numerous benefits of peripheral nerve blocks (PNBs) over general anesthesia (GA) in a variety of surgical procedures, PNBs can be associated with increased post-operative pain if pain medications are not taken correctly (titrated). Unfortunately, this is a common occurrence as patients often have difficulty titrating medications in the absence of direct medical care. PANDA, a smartphone-based postoperative pain management tool, is designed to address this issue by helping patients manage their pain medications. The purpose of this study is to demonstrate the feasibility of this application in patients who are discharged after receiving PNBs. The goal is to identify areas of improvement for the application itself. It is hypothesize that PANDA will be successful in supporting patients' postoperative pain management.

NCT ID: NCT03181438 Recruiting - Clinical trials for Kidney Transplantation

Efficacy Transverse Abdominal Plane (TAP) Block Renal Transplant Surgery

Start date: June 3, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to evaluate the efficacy and safety of transverse abdominal plane block in patients undergoing renal transplant surgery.Adult renal transplant recipients will be prospectively randomized to receive a standard general anesthetic technique supplemented with ropivacaine 0.375% 20 mL TAP block or sham block with 20 mL 0.9% saline. Both groups will receive patient-controlled morphine analgesia. Patient assessment will occur in the postanesthetic care unit and at 1, 2, 4, 6, 12, and 24 hours. The primary outcome is total morphine consumption in the first 24 hours after renal transplantation. Other outcomes asses include pain scores, presence of nausea or vomiting, excessive sedation, and respiratory depression.

NCT ID: NCT02907957 Completed - Clinical trials for Anesthesia, Conduction

Infrared Thermography for Assessment of Caudal Block in Children

Start date: September 2016
Phase: N/A
Study type: Interventional

Regional analgesia via caudal neuraxial blockade provides pain relief for pediatric patients following urological and lower extremity procedures. The injection of local anesthetic into the caudal epidural space causes a sensory loss. This sympathetic blockade in turn causes a vasodilation, or increased blood flow, to the lower extremities. The purpose of this study is to determine whether the FLIR ONE thermographic camera, a smartphone attachment which utilizes an application ("app") to measure the temperature at a site on an image of the lower extremity, will be able to differentiate between caudal, non-caudal, and failed caudal images.

NCT ID: NCT02864602 Completed - Clinical trials for Anesthesia, Conduction

IV Dexamethasone for Prolongation of Peripheral Nerve Block

Start date: November 12, 2016
Phase: Phase 3
Study type: Interventional

This is a volunteer study examining the effect of different doses of IV dexamethasone on prolongation of median nerve block in the forearm.

NCT ID: NCT02589054 Completed - Nerve Block Clinical Trials

Regional Changes in Upper Limb Perfusion Following Brachial Plexus Block: A Pilot Study

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

Ultrasound-guided regional anesthesia is increasingly being used in the modern surgical environment to provide specific intraoperative anesthesia and postoperative analgesia. Infiltration of local anesthesics around peripheral nerves firs blocks sympathetic, then sensory, then motor nerve function. Sympathectomy-induced vasodilation following brachial plexus block results in increased skin temperature and arterial flow within minutes. Although it has not been shown to reliably increase diameter or cross-sectional area of distal arteries, brachial plexus block does change the pattern and quantity of blood flow to the hand. Given that the magnitude of change of flow cannot be attributed to vessel radius, the investigators suspect that the more laminar fluid dynamics are due to vascular tone. The investigators study aims to quantify alterations in physiology and peripheral vasodilator response. The investigators anticipate that axially block will significantly improve regional blood flow.

NCT ID: NCT02457442 Completed - Drug Interactions Clinical Trials

Interaction of Sevoflurane Propofol and Remifentanil in Anesthesia for Laparoscopic Surgery

SPRV
Start date: December 2015
Phase: Phase 4
Study type: Interventional

Recently a new model for the interaction of sevoflurane propofol and remifentanil was developed. The potency of any combination of the three drugs is defined as probability that a subject tolerates laryngoscopy without movement response. The model allows to compare the potency of intravenous and inhalation anesthetics. If the model is valid also for other stimuli than laryngoscopy and for other responses (e.g. blood pressure or heart rate increase upon stimulation). If the model is valid equipotent concentrations of sevoflurane and propofol the same remifentanil concentration would be sufficient to suppress hemodynamic response to a given stimulus. This will be investigated it the study.

NCT ID: NCT02289937 Completed - Pain, Postoperative Clinical Trials

Effect of a Lateral Nerve of the Thigh Block on Postoperative Pain After Total Hip Replacement Surgery

Start date: March 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study was to evaluate the analgesic efficacy of the nervus cutaneous femoral lateralis (NCFL) blockade on postoperative pain after total hip replacement surgery. The NCFL-block is a pure sensory block. We hypothesized that the NCFL-block would reduced the postoperative pain without delaying mobilization.

NCT ID: NCT00636974 Completed - Surgery Clinical Trials

A Randomised Comparison on the Dose Requirement Between, Levobupivacaine, Ropivacaine and Bupivacaine in Intrathecal Anaesthesia

Start date: January 2006
Phase: N/A
Study type: Interventional

To determine and compare the effective intrathecal dose of levobupivacaine, ropivacaine and bupivacaine for 50% of patients in lower limb surgery

NCT ID: NCT00523289 Active, not recruiting - Anesthetics, Local Clinical Trials

Cardiovascular Safety Research: Bupivacaine With Vasoconstrictor Versus Ropivacaine in Brachial Plexus Block

Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if bupivacaine (75% levobupivacaine plus 25% racemic bupivacaine) with vasoconstrictor is effective and safety as ropivacaine in brachial plexus block for orthopedic surgery.

NCT ID: NCT00445016 Active, not recruiting - Nerve Block Clinical Trials

Neurologic Complications in Peripheral Regional Anesthesia - An Evaluation Based on a Standardized Protocol

Start date: May 2008
Phase: N/A
Study type: Observational

To evaluate the incidence of neurologic complications as a consequence of peripheral regional anesthesia, all patients receiving peripheral nerve blocks will be evaluated according to a standardized protocol screening pain, motoric and sensory function recovering to defined periods, and according to a study protocol defining the items.