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Post-cardiac Surgery clinical trials

View clinical trials related to Post-cardiac Surgery.

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NCT ID: NCT03353155 Completed - Clinical trials for Post-cardiac Surgery

Effectiveness of Transitional Care Services

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

The National University Hospital System has designed and is piloting an improved post-discharge care programme called CareHub for patients undergoing cardiac surgery. CareHub is a post-discharge care programme that is designed to streamline and better coordinate current programmes for patients at high risk of readmission. To assess the clinical and cost-effectiveness of CareHub, our team will randomly assign patients to a usual care setting or CareHub setting, and measure clinical outcomes, patient satisfaction, readmissions, and length of stay through 6 months post-discharge in both groups.Patients enrolled in both groups will receive post-discharge care for six months after discharge. CareHub patients will receive a single point of contact for access to usual care services. Recruitment for this pilot will be from 20 April 2016 - approximately late October 2016, and the CareHub team will provide 6 months of post-discharge support. The entire pilot will thus run from 20 April 2016 - April / May 2017, with data collection extending 6 months after the last patient is enrolled.

NCT ID: NCT03270774 Completed - Sepsis Clinical Trials

Central Venous Catheter Colonisation Among Critically Ill Patients in Intensive Care Units

Start date: April 19, 2016
Phase: N/A
Study type: Observational

Background: Central Venous catheter insertion technique and indwelling time are major risk factors for CVC colonisation. Colonisation occurs through microbial migration and biofilm formation along the catheter insertion tract. This study set out to determine the prevalence and associated factors for central venous catheter colonisation among critically ill patient. No data exists in this clinical setting addressing this topic. Methods: The study population included 100 participants with central venous catheters in situ for at least 24 hours. Catheter tip (distal 5-cm segment) and blood cultures (10mls peripheral blood) were obtained at the time of catheter removal.

NCT ID: NCT03025659 Completed - Clinical trials for Post-cardiac Surgery

Lactate Acidosis in Postoperative Hearts

Start date: May 28, 2017
Phase:
Study type: Observational

This is a single-center, observational study. Investigators aim to characterize the metabolism of lactate in children over the first forty-eight hours following cardiac surgery. Blood samples will be obtained up to 12 timepoints. Samples will be analyzed for concentration of pyruvate. Results will be compared to standard of care laboratory results for lactate and other direct and indirect measures of cardiac output.

NCT ID: NCT02829203 Completed - Clinical trials for Post Cardiac Surgery

Pre-Frailty Risk in Cardiovascular Surgery

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

Frailty is an important risk factor for cardiovascular disease (CVD), recent data has shown significant association between pre-frailty and the risk of incident for CVD, irrespective of any classical cardiometabolic risk factors, suggesting that targeting pre-frailty as a potentially reversible risk factor for CVD in the elderly. Patients with high levels of frailty have an increased risk in post-operative period, with more time in mechanical ventilation, length of stay and complications (stroke and death) compared to patients with low frailty levels. The investigators hypothesized that pre-frailty patients also have a higher surgical risk compared to no-frailty patients.

NCT ID: NCT02659982 Completed - Clinical trials for Post Cardiac Surgery

Evaluation of EarlySense Home Care Tele-monitoring Device -For Early Detection of Deterioration For Cardiac Patients at Home

Start date: April 2015
Phase: N/A
Study type: Observational

The aim of this study is to evaluate the relevance of the information as provided by the EarlySense Home care Tele-monitoring system can provide relevant flagging information for clinicians to identify the patients at higher risk to proactively assess patients' condition

NCT ID: NCT02569008 Completed - Clinical trials for Post Cardiac Surgery

Minimal Volume for Fluid Challenge in Post-operative Patients

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

This study evaluate the effect of different doses of crystalloids on the changes on cardiac output (CO) and on the proportion of responders and non-responders and aims to determine the minimal volume required to increase the mean systemic filling pressures (Pmsf) in post-cardiac surgical patients.

NCT ID: NCT01941667 Completed - Clinical trials for Congenital Heart Disease

Transitional Telehealth Home Care: REACH

Start date: July 2012
Phase: N/A
Study type: Interventional

The investigators want to determine if additional, increased contact with infants and families discharged to home after cardiac surgery improves infant and parent outcomes as compared to usual care.

NCT ID: NCT01662141 Completed - Clinical trials for Post Cardiac Surgery

Measure Cardiac Output Using Ultrasound Dilution in Mechanically Ventilated Children

Start date: February 2010
Phase: N/A
Study type: Observational

The measurement of cardiac output (CO) and hemodynamic pressures are vital for proper management of severely hemodynamic compromised patients. A new ultrasound dilution method (COstatus) for cardiac output measurement has been developed.

NCT ID: NCT01647178 Completed - Clinical trials for Post Cardiac Surgery

TORQ Clinical Study

TORQClin
Start date: March 2012
Phase: N/A
Study type: Interventional

The proposed trial is to evaluate the use of the TORQ closure assistance device and how it affects pain in the sternum, breathing and quality of life compared to traditional use of needle drivers or similar to close sternal wires.