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Surgical Procedures, Operative clinical trials

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NCT ID: NCT02768831 Completed - Clinical trials for Surgical Procedures, Operative

ETT Cuff Leak: TV Ratios

Start date: August 17, 2020
Phase: N/A
Study type: Interventional

In the past 5 years cuffed endotracheal tubes (ETT) have become the standard of care in pediatrics. However, hyperinflation of the cuff can compromise the tracheal mucosal perfusion while an inadequate seal may impact ventilation and potentially increase the risk of aspiration. Hence, the goal after placement of a cuffed ETT is to create a safe and effective tracheal seal. The two ways to measure that are to hold CPAP while listening for an audible leak and measuring the difference between the inspired and expired tidal volumes (TV). This is a prospective study to compare these two methods used to create a tracheal seal and measure the intracuff pressure after a satisfactory tracheal seal is established.

NCT ID: NCT02599233 Completed - Pain Clinical Trials

Characterization of Post-operative Pain Trajectories Over Seven Days and Links With Chronicity

PATCH
Start date: March 2016
Phase: N/A
Study type: Observational

The main objective of this study is to establish the postoperative "pain pathways" observed from D1 to D7 in the context of the current management after orthopedic, digestive, obstetrics and gynecology, urology, neurosurgery, vascular and thoracicn surgeries.

NCT ID: NCT02353182 Completed - Clinical trials for Surgical Procedures, Operative

The T REX Pilot Study: a Study to Investigate the Use of an Alternative Anaesthetic in Infants.

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

Animal studies suggest general anaesthetics harm the developing brain. It is unclear if these findings are relevant to humans but the issue has become a major concern. Recent data have found that monkeys exposed to anaesthesia as infants grow up to have slower learning than those not exposed. The aim of the TREX pilot study is to determine the feasibility of an alternative anaesthetic regimen for lower abdominal/lower extremity surgery in infants 1-12 months of age.

NCT ID: NCT02189642 Completed - Clinical trials for Surgical Procedures, Operative

Boston Children's Hospital Post Anesthesia Care Unit Outcomes Study

Start date: July 13, 2013
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the quality of outcomes in the Post Anesthesia Care Unit (PACU) at BCH and to identify preoperative demographic and behavioral data as well as intraoperative and anesthetic predictors of adverse PACU outcomes. The investigators hypothesize quality of PACU outcomes will correlate with preoperative demographic and behavioral characteristics as well as intraoperative and anesthetic procedures/techniques. This study will help the investigators improve post anesthetic care quality and create a higher level of satisfaction for patients, family, and health care providers.

NCT ID: NCT02179112 Completed - Clinical trials for Surgical Procedures, Operative

Determining Universal Processes Related to Best Outcome in Emergency Gastrointestinal Surgery: an International Evaluation

GlobalSurg-1
Start date: July 2014
Phase:
Study type: Observational [Patient Registry]

A multicentre, international evaluation of emergency abdominal surgery to establish surgical outcomes and identify common, modifiable best practice processes.

NCT ID: NCT01929928 Completed - Clinical trials for Surgical Procedures, Operative

Evaluation of Efficacy and Accuracy of a Cordless Ultrasonic Dissection System

SCUD
Start date: January 2013
Phase:
Study type: Observational

The purpose of this study is to test the efficacy of a new cordless ultrasonic dissection system.

NCT ID: NCT01865513 Completed - Anaesthesia Clinical Trials

POPULAR: POst-operative PULmonary Complications After Use of Muscle Relaxants in Europe

POPULAR
Start date: June 2014
Phase: N/A
Study type: Observational

International multicenter observational study of a random-sample cohort of patients undergoing any in-hospital surgical procedure under general or regional anaesthesia during a continued 14-day period of recruitment. Primary hypothesis of this study is that the use of muscle relaxants, their reversal agents, or neuromuscular monitoring increases the incidence of postoperative pulmonary complications. The secondary hypothesis is that the use of muscle relaxants increases in-hospital mortality.

NCT ID: NCT01082614 Completed - Clinical trials for Surgical Procedures, Operative

Arterial Pulse Waveform Contour Analysis for Intraoperative Goal Directed Therapy in Major Abdominal Surgery

Start date: August 2009
Phase: N/A
Study type: Interventional

This study evaluates whether using information from a special arterial blood pressure monitor to guide how much fluid is given during surgery changes how long a patient stays in the hospital after the surgery. There is scientific evidence from using similar information from different devices that this technique might allow us to do a better job giving fluids during surgery and that this may be associated with shorter hospital stay after surgery.

NCT ID: NCT00918437 Completed - Quality of Life Clinical Trials

Postoperative Pain Course After Uvulopalatoplasty

Start date: June 2005
Phase: N/A
Study type: Observational

The aim of this study is to determine the postoperative course including effects on the quality of life following soft palate surgery with radiofrequency knife (RAUP).

NCT ID: NCT00888940 Completed - Clinical trials for Surgical Procedures, Operative

Outcomes and Safety Trial Investigating Ecallantide's Effect on Reducing Surgical Blood Loss Volume in Subjects at High Risk of Bleeding Exposed to Cardio-pulmonary Bypass During Cardiac Surgery

CONSERV-2
Start date: June 2009
Phase: Phase 2
Study type: Interventional

A Phase 2 Randomized Double-Blind Active-Controlled Study in Subjects Exposed to Cardio-pulmonary Bypass During Cardiac Surgery at High Risk of Bleeding