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Surgical Procedures, Operative clinical trials

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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 Recruiting - 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: N/A
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: NCT01524276 Recruiting - Clinical trials for Coronary Artery Disease

Product Surveillance Registry

PSR
Start date: January 2012
Phase:
Study type: Observational

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

NCT ID: NCT01124474 Terminated - Clinical trials for Surgical Procedures, Operative

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

Start date: December 2010
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 a shorter hospital stay after surgery.

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: NCT00987883 Recruiting - Malnutrition Clinical Trials

The Impact of Perioperational Malnutrition on the Cost on Gastroenterological Cancer Patients

Start date: April 2009
Phase: N/A
Study type: Observational

Undernutrition is a state marked by energy and/or protein intake deficiency or mal-absorption, and is often described as protein energy malnutrition (PEM). Malnutrition is common in hospitalized patients worldwide. The prevalence of malnutrition in hospitalized patients range from 20% - 50%, depends on the varieties of diseases, health system, population and assessment tools. It is well documented in Western countries that malnutrition affects clinical outcomes negatively. Compared with well-nourished patients, patients with malnutrition stay longer in hospitals and related cost is significantly higher. There is increasing evidence which indicates that appropriate nutrition support (e.g., standardized nutrition screening procedures, delivering nutrients with appropriate path, etc) may improve clinical outcome on malnutrition, along with cost saving. To date, there is no study to document specifically the impact of malnutrition and related nutrition support on the health economics in China. Considering China now is on its way to establish public health security system and a diagnosis-related grouping system, the understanding of the cost effectiveness of nutrition support under the current clinical conditions is crucial. This study aims to investigate the prevalence of perioperational malnutrition in gastroenterological cancer patient, the nutrition support status and related health economic effects.

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).