Post Cardiac Surgery

7

Review clinical trials related to Post Cardiac Surgery. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

MedlyPeds Feasibility Study

SickKids and UHN have developed MedlyPeds which is a smart phone application designed to remotely monitor patients with heart disease. This is a feasibility study which will enroll up to 30 patients with different types of heart disease to see which patient types may benefit the most from MedlyPeds if it were to be used for clinical monitoring. The study is gathering feedback about the app from patients, parents and clinicians to confirm how it needs to be modified to better serve the purpose in a future trial.

Participants needed: 30
Trial details
Age: 8-18Biological sex: AllType: InterventionalSponsor: The Hospital for Sick ChildrenUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Consent provided. [+7]

Unable to read or write in English. [+1]

Status: Not yet recruiting

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

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.

Participants needed: 50
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: University of CalgaryUpdated: Jun 3, 2026
Eligibility criteria

Age >/=18 years [+2]

LVAD insertion or heart transplantation [+22]

Status: Not yet recruiting

Effect of Neuromuscular Electrical Stimulation on Phrenic Nerve Regeneration Post Cardiac Surgeries

This study will be conducted to investigate the effect of neuromuscular electrical stimulation on phrenic regeneration post cardiac surgery

Participants needed: 60
Trial details
Age: 25-45Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Oct 1, 2024Locations: 1
Eligibility criteria

Patients post cardiac surgery (coronary artery bypass graft, valve repair or rep... [+7]

Patients with rib fracture. [+4]

Status: Recruiting

Intravenous Acetaminophen After Cardiac Surgery - Definitive Study

Double blind, double dummy trial of the use of IV acetaminophen versus oral acetaminophen for the prevention of delirium after cardiac surgery. The underlying hypothesis is that better pain control and less use of narcotics will lead to a lower incidence of delirium from day 1 to 7 following cardiac surgery. Other important secondary outcomes are the total use of narcotics, ICU and hospital stay, improved cognitive function at 6 months and 1 year post surgery, NSAID use at each centre and associated NSAID complications.

Participants needed: 1,100
Trial details
Phase: Phase 4Age: 18+Biological sex: AllType: InterventionalSponsor: McGill University Health Centre/Research Institute of the McGill University Health CentreUpdated: Sep 25, 2024Locations: 8
Eligibility criteria

elective cardiac surgery [+2]

Status: Recruiting

Comb Effect of 4-7-8 Breathing Technique and Stationary Cycle on PP, QOL and Dyspnea in Post CABG Patients.

To determine the combined effects of 4-7-8 breathing technique and stationary cycle on physical performance, quality of life and dyspnea in post CABG patients.

Participants needed: 58
Trial details
Age: 40-70Biological sex: AllType: InterventionalSponsor: Riphah International UniversityUpdated: Jun 26, 2024Locations: 1
Eligibility criteria

Patients who underwent a successful CABG (no complications during surgery [+8]

Ventricular Septal defect repair. [+9]

Status: Not yet recruiting

Pharmacokinetics and Modelling of Beta-Lactam in ECMO-VA Patients

The use of antibiotic therapy is common in intensive care units and primarily involves beta-lactams. Its optimal implementation is made difficult by the pharmacokinetic changes inherent in critically ill patients. Despite the current recommendations from the French Society of Anesthesiology and Intensive Care (SFAR) and the French Society of Pharmacology and Therapeutics (SFPT), there are no recommendations on prescription modalities for patients under veno-arterial extracorporeal membrane oxygenation (VA-ECMO). The use of antibiotic therapy is common in VA-ECMO patients and their pharmacokinetic variability factors are then exacerbated. We aim to conduct a prospective, multicenter, interventional study designed to identify predictive factors for failure to achieve therapeutic target circulating concentrations of beta-lactams in patients under VA-ECMO treated with one of the studied beta-lactams

Participants needed: 225
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University Hospital, GrenobleUpdated: Mar 29, 2024Locations: 5
Eligibility criteria

Patients undergoing VA-ECMO [+3]

Subject under administrative or judicial surveillance [+6]

Status: Recruiting

Post-Surgery Extracorporeal Life Support

Extracorporeal Life Support (ECLS) may provide pulmonary and circulatory support for patients with acute heart failure refractory to conventional medical therapy. However, indications and effectiveness of ECLS engagement post-surgery remains a concern. The investigators sought to analyze indications, modality and outcomes of PS-ECLS, to identify predictors of early and midterm survival after PS-ECLS. The investigators have recorded prospectively, and analysed data of 209 consecutive PS-ECLS patients between January 2004 and December 2018. Demographic and clinical data before, during and after PS-ECLS were collected and their influence on hospital mortality and outcomes (early and midterm) will analyse. Multivariate analysis of pre PS-ECLS implantation factors (as age, female sex , insulin-dependent diabetes, pulmonary hypertension, STS, type of surgical procedure data, pre-ECLS blood lactate level) will be made for identify prognostic risk factors of in-hospital mortality. Overall survival will be analysed, at 6 months,1-year and 5-years, respectively and the factors influencing mild/term outcome will be investigated.

Participants needed: 500
Trial details
Age: 18-80Biological sex: AllType: ObservationalSponsor: University of FlorenceUpdated: Apr 28, 2021Locations: 1Duration: 20 Years
Eligibility criteria

Patients underwent cardiac surgery

Age < 18 years