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Anesthesia Complication clinical trials

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NCT ID: NCT04264351 Completed - Clinical trials for Postoperative Delirium

Frailty, Anesthesia and Complications.

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

Objectives: To assess the prevalence of frailty in patients older than 70 y/o in nephrourologic surgery. To study if preoperative frailty is an independent predictor of immediate postoperative complications, after 30 days, 6 months and 1 year of follow-up. To detect if there are other independent risk factors for complications.

NCT ID: NCT04209608 Completed - Clinical trials for Anesthesia Complication

Observational Study on Respiratory Impact of High-frequency Jet Ventilation (JVHF) in Interventional Radiology (RI)

Pulmojet
Start date: March 12, 2020
Phase:
Study type: Observational

Jet ventilation is used in interventional radiology to reduce respiratory movement and facilitate tumor destruction. The purpose of this study is to describe the respiratory impact of this technique

NCT ID: NCT04124757 Recruiting - Clinical trials for Neuromuscular Blockade

Impact of Deep Versus Standard Muscle Relaxation on Intra-operative Safety

EURORELAX
Start date: February 11, 2020
Phase: N/A
Study type: Interventional

Muscle relaxants are routinely applied during anesthesia to facilitate endotracheal intubation and to improve surgical working conditions. Several investigations have shown that a deep neuromuscular block (NMB) improves the surgical working conditions over a moderate NMB and effectively precludes sudden deterioration of the surgical field. However, whether the improvement of surgical working conditions translates into less intra- and postoperative complications remains uncertain. Small prospective or retrospective studies shown an decrease of the incidence of intraoperative adverse events and postoperative complications after a deep NMB. There is a need to confirm these outcome data prospectively, in a large number of patients and clinics and during a variety of surgical procedures.

NCT ID: NCT04005664 Completed - Clinical trials for Cesarean Section Complications

Prophylactic Phenylephrine Co-administration During Caesarean Section

Start date: May 1, 2018
Phase: N/A
Study type: Interventional

This single centre prospective alternating intervention study will aim to compare prophylactic phenylephrine given in the first litre of Ringers lactate as co-load in healthy patients having an elective caesarean section under spinal anaesthesia at Edendale Hospital to the existing national protocol guideline - for the treatment of obstetric spinal hypotension.

NCT ID: NCT03972423 Completed - Anesthesia Clinical Trials

Impact of a Transmission Checklist in Post Anesthesia Care Unit on Immediate Respiratory Complications

TC-IRC
Start date: February 18, 2019
Phase:
Study type: Observational [Patient Registry]

This work highlighted the beneficial role in terms of carers' satisfaction, quantity and quality of information transmitted.

NCT ID: NCT03913858 Completed - Morbid Obesity Clinical Trials

Low Flow Anesthesia in Morbid Obesity

Start date: January 10, 2019
Phase: N/A
Study type: Interventional

In this study to planned to research the efficacy of low-flow anesthesia on patients undergoing sleeve gastrectomy due to morbid obesity on respiratory functions after surgery by examining FEV1 and FVC values and FEV1/FVC ratio.

NCT ID: NCT03910504 Completed - Clinical trials for Neuromuscular Blockade

Anaesthesia With or Without Rocuronium in Intubation and Intraoperative Nerve-monitoring During Thyroid Surgery.

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

In this randomized controlled trial the investigators want to assess if, compared to controls, the administration of one single low-dose of rocuronium would increase the occurrence of absent or weak (i.e. amplitude <100 μV) signal at V1 and R1, indicating a residual NMBA activity. In addition, we also recorded: 1) the occurrence of difficult laryngoscopy; 2) the time-to-intubation; 3) the occurrence of difficult intubation; 4) the number of intubation attempts; 5) the intubation failure rate; 6) the need for oxygenation between intubation attempts; 7) the lowest peripheral saturation in oxygen (SpO2); 8) the number of severe desaturations; 9) the time-to-V1 and 10) the number of post-surgical complications.

NCT ID: NCT03744455 Completed - Clinical trials for Anesthesia Complication

Influence of Resident's Degree of Formation on the Quality of Care Delivered to the Patients.

Start date: September 1, 2018
Phase:
Study type: Observational

The aim of this study is to evaluation the influence of the resident in anesthesiology's degree of formation on the quality of care delivered to the patient.

NCT ID: NCT03438734 Completed - Morbid Obesity Clinical Trials

Comparison of Low Versus Normal Flow Anesthesia on Cerebral Oxygenation and Bispectral Index in Morbidly Obese Patients

CerOxygen
Start date: November 8, 2017
Phase: N/A
Study type: Interventional

Obesity is a chronic disease that affects quality and duration of life negatively. It's not clearly known the effects of low flow anesthesia on cerebral oxygenation with high-risk morbidly obese patients. In this study, it was aimed to compare the effects of general anesthesia with low flow (0,75 L/min) and normal flow (1,5 L/min) on cerebral oxygenation and depth of anesthesia in morbidly obese patients in bariatric surgery.

NCT ID: NCT03312413 Recruiting - Clinical trials for Anesthesia Complication

Efficacy of Dexmedetomidine for Cough Suppression in Patients Undergoing Thyroid Surgery

EDCSTS
Start date: August 10, 2017
Phase: Phase 4
Study type: Interventional

Maintenance of a remifentanil infusion during anesthetic emergence has been reported to decrease the incidence of coughing and thereby help to ensure a smooth emergence. It may, however, cause respiratory depression and possibly delay emergence. The purpose of this study was to investigate the effect of different dose of dexmedetomidine infusion on cough suppression during emergence from general anesthesia in patients undergoing thyroid surgery. American Society of Anesthesiologists physical status I-II adults undergoing elective thyroidectomy under general anesthesia are recruited and randomly allocated to receive dexmedetomidine iv infusion of 0.2μg·kg-1·h-1 (Group D1, n = 100), 0.5μg·kg-1·h-1 (Group D2, n = 100), 0.7μg·kg-1·h-1 (Group D3, n = 100) or saline (Group C, n = 100). Primary outcome is the incidence of coughing during emergence. Second outcomes include severity of coughing, which is assessed using a four-point scale; Ramsay score, Bruggrmann comfort scale score, VAS pain score are recorded. The respiratory rate (RR), heart rate (HR), and mean arterial pressure are also recorded.