Clinical Trials Logo

Cardiopulmonary Bypass clinical trials

View clinical trials related to Cardiopulmonary Bypass.

Filter by:

NCT ID: NCT02675647 Recruiting - Cardiac Surgery Clinical Trials

Heparin Based on Ideal Body Weight for Cardiopulmonary Bypass in Obese Patients

HEPOIRINE
Start date: December 2015
Phase: Phase 4
Study type: Interventional

The optimal heparin regimen during cardiopulmonary bypass (CPB) has not been well established in obese patients. Results of a preview study show that the standard heparin management based on total body weight in obese patients during CPB resulted in excessive heparin level, which could lead to excessive postoperative bleeding. To avoid this overdosing, an initial heparin bolus based on ideal body weight in obese patients was proposed. The main objective of the study is to evaluate the effects of heparin injection, based on ideal body weight, on intraoperative plasma heparin levels and activated coagulation time (ACT) in a population of obese patients, compared to a group of obese patients undergoing CPB surgery with heparin management based of total body weight. The secondary objectives are to evaluate the relationship between heparin level and ACT in each group of patients and at different time points during CPB, and to compare the incidence of bleeding, intraoperative transfusions and complications in the two groups of patients.

NCT ID: NCT01231776 Recruiting - Clinical trials for Heart Valve Diseases

Acupuncture Improves Sleep in Patients Undergoing Cardiopulmonary Bypass

Start date: September 2010
Phase: N/A
Study type: Interventional

Due to various causes, such as brain impairment, environment changes, anxious,et al. patients, who undergo cardiopulmonary bypass, often suffer from poor quality of sleep. In chinese traditional medicine, acupuncture can improve the quality of sleep in patients with sleeping disorder. But it remains acupuncture could improve the quality of sleep in patients with heart operations.

NCT ID: NCT00906906 Recruiting - Clinical trials for Cardiopulmonary Bypass

Validation of Venous Cannulae Flow Ratings

Start date: January 2008
Phase: N/A
Study type: Observational

The purpose of this study is to characterize blood flow in the plastic tubing of a heart-lung bypass machine during heart surgery. Technical specifications provided by the manufacturer do not consider varying hemodynamic conditions such as temperature and hemoglobin levels which affect blood viscosity and ultimately blood flow to and from the patient during heart-lung bypass. The investigator wishes to perform a prospective study of the heart-lung bypass tubing in children that require heart-lung bypass during heart surgery.

NCT ID: NCT00745394 Recruiting - Clinical trials for Cardiopulmonary Bypass

Validation of Near Infrared Spectroscopy (NIRS) During Heart-Lung Bypass in Children

NIRS
Start date: April 2008
Phase: N/A
Study type: Observational

Non-invasive assessment of blood flow to organs has long challenged clinicians. Recently, near infrared spectroscopy (NIRS) has been recognized as a methodology that may achieve this goal. A commercially available NIRS monitor, marketed by Somanetics, Inc., is now in widespread use in the clinical care of pediatric cardiac patients in the operating room and in the intensive care unit post-operatively. When a patch/probe from the monitor is placed on the forehead or lower back, blood oxygen concentration data is obtained which has been found to correlate with actual blood samples taken by IV. The presence of this NIRS data would give the surgeon important feedback about blood flow to important areas like the brain and kidneys during heart surgeries on children and after the operation is completed in the intensive care unit. The investigator wishes to perform a prospective study of the NIRS monitor use with children that need heart surgeries that require heart-lung bypass and sometimes require monitoring in the ICU, post-operatively.

NCT ID: NCT00350441 Recruiting - Clinical trials for Cardiopulmonary Bypass

Does Sildenafil Protect Against Pulmonary Related Complications Following Cardiopulmonary Bypass?

Start date: June 2006
Phase: Phase 4
Study type: Interventional

Does pre-operative administration of Sildenafil (Viagra, Pfizer) reduce the lung injury associated with cardiopulmonary bypass in children undergoing corrective surgical repair of congenital heart disease.

NCT ID: NCT00187967 Recruiting - Clinical trials for Coronary Artery Disease

Cardiopulmonary Bypass (CPB) Pumps and Blood Activation

Start date: January 2005
Phase: N/A
Study type: Interventional

Blood activation induced by cardiopulmonary bypass may compromise the postoperative outcome. The goal of this study is to compare blood activation induced by cardiopulmonary bypass performed with centrifugal pump or roller pump in patients undergoing coronary artery surgery.

NCT ID: NCT00182377 Recruiting - Cardiac Surgery Clinical Trials

Pentastarch Use in Cardiac Surgery

Start date: n/a
Phase: N/A
Study type: Interventional

Patients undergoing cardiac surgery with cardiopulmonary bypass require significant fluid administration. Fluids are used routinely to replace blood lost during and after surgery. Significant amounts of fluid are also used to prime the tubing and components of the cardiopulmonary bypass pump before and during its use. The use of Pentaspan - a synthetic pentastarch - was started because of the restriction of use for blood and blood products, particularly albumin. Pentaspan is usually used after surgery in the Intensive Care Unit (ICU). The impact of the use of pentastarch on coagulation, fluid balance and bleeding are very limited. This study will methodically evaluate the impact of using increasingly greater amounts of pentastarch during surgery on an open heart surgery patient's recovery in particular - is there more bleeding, does his/her blood clot as well, and how much fluid overall is used and excreted?