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Anesthesia Morbidity clinical trials

View clinical trials related to Anesthesia Morbidity.

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NCT ID: NCT03117894 Completed - Anesthesia Clinical Trials

PECS-2 for Breast Surgery

Start date: May 23, 2017
Phase: N/A
Study type: Interventional

There is no consensus regarding which alternative is the best anesthesia for breast surgery, general anesthesia and morphine for postoperative analgesia or a combination of regional anesthesia and general anesthesia that possibly attenuates or abolishes the need for morphine. The current study aims to determine which of the two strategies that is best in relation to postoperative pain, nausea and risk of recurrence of the disease.

NCT ID: NCT03044418 Completed - Anesthesia Clinical Trials

Anesthesia With Endotracheal Laser Tube

Start date: January 1, 2017
Phase:
Study type: Observational [Patient Registry]

The study examines the special endotracheal laser tube during anesthesia of endolaryngeal laser surgery.

NCT ID: NCT03028688 Completed - Clinical trials for Anesthesia Morbidity

HIFLO ENDO-High Flow Nasal Cannula in GI Endoscopy

Start date: June 21, 2017
Phase: N/A
Study type: Interventional

Millions of patients undergo upper GI endoscopy in the United States each year. A large number of these patients have anesthesia to assist with their comfort during the procedure. The majority of patients do not have a protected airway during the procedure, meaning there is no endotracheal tube. Instead the current standard of care is to give supplementary oxygen via nasal cannula. Because patients are deeply sedated or have general anesthesia there is a risk for low oxygen saturation during the procedure, which presents a significant patient safety issue. The purpose of the clinical trial is compare the current anesthesia standard of care against high flow nasal cannula oxygen delivery during anesthesia. The investigator's hypothesis is that high flow nasal cannula oxygen delivery will decrease the frequency with which patients experience hypoxemia during anesthesia for upper GI endoscopy.

NCT ID: NCT02738814 Enrolling by invitation - Child Clinical Trials

Propofol for Treatment on Emergence Agitation

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

This study aimed to verify the effects of propofol for treatment on emergence agitation (EA) after sevoflurane anesthesia in pediatric strabismus surgery.

NCT ID: NCT01963754 Active, not recruiting - Clinical trials for Dental Implant Failed

Compare Subperiosteal and Loco-Regional Anesthesia in Posterior Mandible Dental Implant Installation

Start date: April 1, 2017
Phase: Phase 4
Study type: Interventional

In patients that are going to receive a dental implant in the posterior mandible (distal from canine), does the subperiosteal anesthetic technique with Articaine 1:100.000 4 % Epinephrine compared to the loco-regional one, produces the same analgesia during surgery ?

NCT ID: NCT01740453 Completed - Clinical trials for Respiratory Depression

Effect of Interscalene Block on Ventilatory Function

KTBIS
Start date: January 2012
Phase: Phase 4
Study type: Interventional

Interscalene block with local anesthetic impairs ventilation (unilateral diaphragmatic dysfunction). Single injection of local anesthetic induced transitory dysfunction (< 24h). The investigators hypothesized that continuous interscalene block would prolonged ventilatory impairment

NCT ID: NCT01680471 Completed - Child Clinical Trials

A Study on the Effects of Midazolam on Delirium After Sevoflurane Anesthesia in Pediatric Strabismus Surgery

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

Sevoflurane with its rapid induction and emergence, hemodynamic stability, and nonirritating airway properties, has acquired widespread acceptance in children. However, sevoflurane has been reported to be associated with emergence agitation in children, with a reported incidence of up to 80%. The purpose of this study is to verify that the prophylactic use of midazolam, which is a GABA A receptor inhibitor, given five minutes before the end of strabismus surgery reduces the incidence of emergence agitation after sevoflurane anesthesia in children. Simultaneously, this study aims to find out the proper dose of midazolam with minimum disturbance to patient's emergence time.