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Post-cardiac Surgery clinical trials

View clinical trials related to Post-cardiac Surgery.

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NCT ID: NCT05644418 Completed - Clinical trials for Post-cardiac Surgery

EIT During FCV in the Intensive Care Unit

Start date: February 22, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to study the effects of Flow Controlled Ventilation (FCV) following conventional mechanical ventilation (Pressure or Volume Controlled Ventilation) in postcardiac surgery ICU-patients to allow for future power calculations and to obtain experience with FCV. The main questions it aims to answer are: - What is the effect of FCV on the lung volume measured by Electrical Impedance Tomography (EIT)? - What is the effect of FCV on the minute volume? - What is the effect of FCV on the mechanical power and dissipated energy? Participants will be ventilated with PCV at baseline and then switched to FCV for 90 minutes while the lung volume, minute volume and mechanical power and dissipated energy levels are measured.

NCT ID: NCT05587803 Completed - Deep Sedation Clinical Trials

Comparison of 2 Depth of Sedation Indices in the Intensive Care Unit

PSIWAV
Start date: May 9, 2022
Phase: N/A
Study type: Interventional

In the intensive care unit of the Free University hospital of Brussels, sedated patients are standardly monitored with the Masimo SEDline device to see how deeply a patient is asleep. During this study we want to attach 1 extra device to 30 sedated patients, lying in the intensive care unit. This device, called the NeuroSENSE brain monitor from Neurowave systems, uses a different scale to indicate the ideal depth of sedation. In total, both devices will be hung on a patient for 2 times 35 minutes. At minute 33, a RASS score will be determined in each patient. This score will be determined by talking to the patient or administering a pain stimulus. Based on the reaction of the patient an estimation can be made how deeply a patient is sleeping. Our goal is to find out which device correlates best with the effective clinical state of the patient.

NCT ID: NCT05285098 Recruiting - Clinical trials for Post-cardiac Surgery

Leipzig FAST-TRACK Over 15 Years for Cardiac Surgical Patients

Start date: April 1, 2021
Phase:
Study type: Observational

Since November 2005, we are running a specialized post anesthetic care unit (PACU) in our tertiary, university affiliated high-volume heart centre. In our concept, we are bypassing ICU admission completely. The fast-track concept was initially applied to pre-selected elective patients undergoing low-risk operations. However, promising outcomes led to a more widespread utilization with more complex procedures. The aim of this study is to analyse the fast track evolutions.

NCT ID: NCT05044559 Completed - Clinical trials for Post-cardiac Surgery

Continuous Positive Air Way Pressure in Cardiac Rehabilitation After CABG

Start date: July 15, 2019
Phase: N/A
Study type: Interventional

Different studies reported that CPAP is effective to prevent respiratory complication in post CABG patient and have greater impact on walking time, ventilatory function and breathing pattern.

NCT ID: NCT05023083 Completed - Clinical trials for Post-cardiac Surgery

Cross Cultural Adaptation of Functional Status Questionnaire in Urdu Language in CABG Patients

Start date: May 23, 2021
Phase:
Study type: Observational [Patient Registry]

Aim of the study is to create an Urdu version of FSQ which will be of great importance for further research in field of cardiopulmonary physiotherapy, specially to make comparison across the population. We therefor aimed to develop a linguistically validated and reliable Urdu version of FSQ.

NCT ID: NCT04980742 Recruiting - Prognosis Clinical Trials

Perioperative Risk Factors of Outcomes for Cardiac Surgery: A Retrospective Study

Start date: July 1, 2017
Phase:
Study type: Observational

Based on a review of about 10,000 patients undergoing cardiac surgery under CPB in West China Hospital of Sichuan University and the Second Affiliated Hospital of Zhejiang University, we try to evalute the effect of blood transfusion on outcomes in cardiac surgery.

NCT ID: NCT04782635 Completed - Clinical trials for Post-cardiac Surgery

Effect of Artificial Intelligence on Nutritional Status of Children Post Cardiac Surgery

Start date: March 25, 2021
Phase: N/A
Study type: Interventional

The objective of the study will be to assess the effect of artificial intelligence on nutritional status of children post cardiac surgery in comparison to usual care group.To assess usefulness of diet related mobile application in comparison to usual care group.To identify diet related problems among children post cardiac surgery in both groups (usual care group and intervention group ).

NCT ID: NCT04748991 Not yet recruiting - Atrial Fibrillation Clinical Trials

Vernakalant Versus Amiodarone for Post-operative Atrial Fibrillation in Cardiac Surgery Patients

Start date: September 2024
Phase: Phase 3
Study type: Interventional

Post-operative atrial fibrillation is a common problem post cardiac surgery with rates exceeding 30%. Atrial fibrillation has multiple adverse effects on cardiac hemodynamics and can lead to hypotension, diminished end organ perfusion and lengthen the stay in ICU. Amiodarone is the medication of choice used for pharmacological cardioversion and can be used with vasoactive medications. Intravenous amiodarone is associated with hypotension and end organ perfusion requiring escalation in vasoactive support. Vernakalant is novel anti-arrhythmic agent approved in Canada for cardioversion of atrial fibrillation that primarily works on atrial channels and has no effect on contractility or vasodilation. Clinical trials have proved good efficacy of Vernakalant in conversion of paroxysmal atrial fibrillation however there is no comparison of Amiodarone to Vernakalant in post-operative cardiac surgery. We plan to perform a clinical trial comparing Vernakalant to amiodarone in post-cardiac surgery patients with a primary outcome of cardioversion at 90 minutes. Secondary outcomes will follow duration of vasoactive medications, days in ICU and economics.

NCT ID: NCT04745468 Completed - Clinical trials for Post-cardiac Surgery

Study on CRP Apheresis After Coronary Bypass Surgery

CABY1
Start date: March 21, 2018
Phase: N/A
Study type: Interventional

The CABY1 study is conducted open, controlled, randomized and monocentric. The efficacy and tolerability of CRP apheresis in patients undergoing elective primary coronary bypass surgery is investigated.

NCT ID: NCT04674865 Completed - Clinical trials for Post-cardiac Surgery

Alternate Nostril Breathing on Cardiorespiratory Functions in Phase 1 Post CABG Patients

Start date: September 25, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to investigate effects of Anulom vilom pranayama/ Alternate nasal breathing (ANB) on cardio-respiratory parameters including vitals i.e. heart rate, blood pressure, chest expansion, arterial blood gases (ABGs), pulmonary function test and functional capacity in phase 1 post CABG patients. This study will help Cardiopulmonary physiotherapists to incorporate evidence based protocols for Coronary Artery Bypass Graft Surgery (CABG) in phase 1 of cardiac rehabilitation.