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Respiratory Complication clinical trials

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NCT ID: NCT03255356 Not yet recruiting - Anesthesia, General Clinical Trials

Ventilation in Cardiac Surgery

VENICE
Start date: November 1, 2017
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate prospectively ventilatory practices in the perioperative cardiac surgery period.

NCT ID: NCT03218215 Completed - Clinical trials for Neuromuscular Diseases

Monitoring Mechanical Assisted Cough

MONICA
Start date: May 1, 2015
Phase: N/A
Study type: Observational

Background Mechanical assistance cough for patients with neuromuscular disorders (NMD) are known, but there is no adaptation model established. Currently is performed subjectively by the physiotherapist following the pressures recommended in the current literature as optimal (±40CmH2O). To check is these pressures are the most optimal pressures to achieve the better peak cough flow (PCF) monitoring cough assist (Mechanical insuffllation-exsuflattion MI-E) maneuvers and analyzing pressure- flow / time curves Adults with MI-E criteria (PCFbaseline <160 l /min). A pneumotachograph, PeakAnalysis software and nasobucal mask were used to monitor and analyze flow/time curves. Protocol included 9 PCF values in each patient: 1 baseline, 4 related with inspiratory pressure in sequential increase of 10 cmH2O (10 to 40 cmH2O) and 4 adding expiratory pressures (±10 to ±40cmH2O)

NCT ID: NCT03198208 Active, not recruiting - Surgery Clinical Trials

Intraoperative Fentanyl Dose on Respiratory Complications

Start date: January 1, 2007
Phase: N/A
Study type: Observational [Patient Registry]

Fentanyl is the most commonly used opioid during anesthesia at Massachusetts General Hospital. Compared to other opioids, e.g. sulfentanil and remifentanil, fentanyl's pharmacokinetic properties are more problematic as the context sensitive half-time increases with duration of fentanyl infusion. This may lead to respiratory complications particularly in patients who receive fentanyl for surgical procedures of long duration. Considering the common use of fentanyl during surgery and its duration of action that is hard to predict during long surgical procedures, we will evaluate the association between intraoperative fentanyl dose and postoperative respiratory complications within 3 days of surgery.

NCT ID: NCT03105739 Completed - Clinical trials for Respiratory Complication

Timing of Withdrawal of the Laryngeal Mask Airway (LMA) in Children

Start date: October 5, 2016
Phase: N/A
Study type: Interventional

The purpose of this prospective, randomized study was to compare the incidence of adverse events associated with removal of the LMA either in deeply anesthetised or awake patients.

NCT ID: NCT03102619 Completed - Clinical trials for Postoperative Complications

Wireless Assessment of Respiratory and Circulatory Distress; A Pilot Study

WARD
Start date: March 23, 2017
Phase: N/A
Study type: Observational

Postoperative observation of patients is based on the Early Warning Score (EWS). By using continuous wireless monitoring of vital parameters it may be possible to predict the risk of complications after abdominal cancer surgery. The object of this pilot study is to test the equipment and methods for the next phases. Patients will be monitored for 4 days postoperatively and data is analyzed retrospectively. Vital parameters are monitored with ECG, blood pressure monitor and pulseoximetry. In the analysis the investigators will compare the results from the continuous monitoring to the measurements made by the nurses and registered in the EWS. The primary outcomes for the pilot study are the frequency of measurements resulting in a single parameter score of 3 according to the EWS algorithm.

NCT ID: NCT03072784 Completed - Clinical trials for Respiratory Complication

Aortic Cross Clamping Time, and Postoperative Respiratory Function

Start date: February 1, 2015
Phase: N/A
Study type: Interventional

Does the duration of cardiopulmonary bypass, and aortic cross clamping affects the post operative pulmonary function.

NCT ID: NCT03056885 Completed - Clinical trials for Inflammatory Response

Inflammatory Local Response During OLV: Protective vs Conventional Ventilation Strategy

Start date: November 2, 2015
Phase: N/A
Study type: Interventional

This study evaluates the local cytokine inflammatory response during one lung ventilation in patients undergoing pulmonary lobectomy or wedge resection. We compare two different ventilation strategies: a conventional strategy with a protective strategy.

NCT ID: NCT03010852 Completed - Clinical trials for Respiratory Complication

Focused Incentive Spirometry Monitoring to Reduce Postoperative Oxygen Therapy and Respiratory Complications After Bariatric Surgery

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

Postoperative (PO) hypoventilation, atelectasis and hypoxemia after bariatric surgery are common and multifactorial, contributing to prolonged oxygen (O2) therapy after surgery and even at hospital discharge. Incentive spirometry (IS) is recommended postoperatively but its success in preventing postoperative atelectasis and hypoxemia (POH) heavily depends on patient compliance with IS effort and frequency. The investigators hypothesize that a focused education preoperatively on IS for POH and intensive monitoring of patient compliance with IS therapy in the early postoperative period shortens postoperative oxygen therapy, decreases POH episodes, and improves respiratory outcomes after bariatric surgery, compared to patients receiving standard of care.

NCT ID: NCT02512770 Completed - Clinical trials for Hemodynamic Instability

Hemodynamic and Respiratory Effects of Esophageal Dilation in Children

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

The aim of this study compares hemodynamic and respiratory changes and complications in children who undergoing endoscopy for esophageal balloon dilatation and endoscopy for only control.

NCT ID: NCT02037516 Completed - Morbid Obesity Clinical Trials

Does Residual Muscular Weakness Lead to an Increase in Respiratory Complications in Bariatric Patients?

Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if residual weakness after weight loss surgery leads to an increased risk of respiratory complications in the postoperative period.