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Surgical Procedures, Operative clinical trials

View clinical trials related to Surgical Procedures, Operative.

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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: 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

NCT ID: NCT00840593 Completed - Clinical trials for Surgical Procedures, Operative

A Prospective, Randomised Long-term Follow-up of Operative Versus Non-operative Treatment of Gr. 3 Acromioclavicular Dislocation

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

The purpose of this study is to compare the long-term clinical and radiological results of operative and conservative treatment of Tossy type 3 acromio-clavicular dislocation.

NCT ID: NCT00816023 Completed - Clinical trials for Surgical Procedures, Operative

A Dose-ranging Safety and Efficacy Study of Ecallantide to Reduce Surgical Blood Loss Volume

CONSERV-1
Start date: March 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the efficacy and identify the optimal dose(s) of ecallantide in reducing blood loss in subjects undergoing coronary artery bypass surgery including the use of cardio pulmonary bypass.

NCT ID: NCT00581139 Completed - Pain, Postoperative Clinical Trials

Psychological Influences on Postoperative Recovery

NIH
Start date: April 2003
Phase: Phase 2
Study type: Interventional

The primary hypothesis tested in this project is that the preoperative behavioral stress response predicts postoperative behavioral and clinical recovery of children undergoing surgery.