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Condition

Cardiac Surgery Clinical Trials

Studies of cardiac surgery, matched by condition name and medical subject headings. Start with those open to enrolment.

5,514 registered studies

In numbers

Open to volunteers
887
Active
1,050
With results posted
445
All registered
5,514

Open to volunteers: recruiting, not yet recruiting or enrolling by invitation. Active adds studies under way that have stopped recruiting.

Open to volunteers

All 887
  • Pain, Postoperative

    Gabapentin to Reduce Opioid Use Postoperatively (GROUP) in Children

    • Recruiting
    • Age: Up to 17 years
    • Phase 2/3

    The primary objective of this study is to determine if the peri and post operative use of gabapentin in children reduces the need for narcotics after thoracic surgery.

    Trial name
    NCT04724252
    Testing
    Gabapentin
    Where
    United States
    Volunteers
    60 people
    Sponsor
    University of California, Davis
    Can I take part? NCT04724252
  • Aortic Regurgitation, Aortic Valve Insufficiency

    ARTIST: Aortic Regurgitation Trial Investigating Surgery Versus Trilogy™

    • Recruiting
    • Age: All ages
    • Medical device

    To demonstrate non-inferiority of the Trilogy Transcatheter Heart Valve (THV) System compared with surgical aortic valve replacement (SAVR) for treatment of subjects with clinically significant native aortic regurgitation (AR)

    Conditions
    Aortic Regurgitation, Aortic Valve Insufficiency, Aortic Insufficiency
    Trial name
    ARTIST (NCT06608823)
    Testing
    Transcatheter Aortic Valve Replacement (TAVR) using Trilogy THV System, SAVR
    Where
    38 sites in United States
    Volunteers
    1,016 people
    Sponsor
    JenaValve Technology, Inc.
    Can I take part? ARTIST
  • Tonsillectomy and Adenotonsillectomy in Children

    Boyle-Davis Mouth Gag Timing in Pediatric Tonsil Surgery

    • Not yet recruiting
    • Age: 3 to 12 years
    • Surgery or procedure

    The aim of this randomized controlled trial is to compare the effects of placing the Boyle-Davis mouth gag 3 minutes versus 10 minutes after endotracheal intubation on the hemodynamic response in pediatric patients aged 3-12…

    Trial name
    NCT07889206
    Testing
    Early Boyle-Davis Mouth Gag Placement, Delayed Boyle-Davis Mouth Gag Placement
    Volunteers
    40 people
    Sponsor
    Yahyali State Hospital
    Can I take part? NCT07889206
  • Atrial Functional, Mitral Regurgitation (MR)

    PRECISE-AFMR I: Transcatheter Mitral Valve Edge-to-Edge Repair for Atrial Functional Mitral Regurgitation in Patients at High Surgical Risk

    • Recruiting
    • Age: 18 years and older
    • Medical device

    Atrial functional mitral regurgitation (AFMR) develops when enlargement and remodeling of the left atrium and mitral annulus prevent the mitral valve leaflets from closing completely, allowing blood to leak backward through the…

    Trial name
    PRECISE-AFMR I (NCT07741253)
    Testing
    Transcatheter Edge-to-Edge Repair
    Where
    China
    Volunteers
    182 people
    Sponsor
    China National Center for Cardiovascular Diseases
  • Glucose Metabolism Disorders (Including Diabetes Mellitus)

    Continuous Glucose Monitoring in Patients Undergoing Cardiopulmonary Bypass

    • Not yet recruiting
    • Age: 18 years and older
    • Medical device

    The purpose of this research study is to test the accuracy of the Dexcom continuous glucose monitoring device during the cardiothoracic surgical procedure and recovery period in the Cardiac Intensive Care Unit.

    Trial name
    NCT06861881
    Testing
    Dexcom G7 Continuous Glucose Monitor
    Where
    United States
    Volunteers
    100 people
    Sponsor
    Wake Forest University Health Sciences
    Can I take part? NCT06861881
  • Cardiovascular Diseases

    Wearable Ultrasound for Cardiac Monitoring During Surgery and in Intensive Care

    • Not yet recruiting
    • Age: All ages
    • Medical device

    This study aims to evaluate the accuracy, feasibility, and clinical usefulness of a wearable ultrasound imaging system for cardiac monitoring during perioperative care and in intensive care units (ICUs).

    Trial name
    NCT07891052
    Testing
    Wearable Ultrasound Imaging System
    Volunteers
    600 people
    Sponsor
    China National Center for Cardiovascular Diseases
    Can I take part? NCT07891052
  • Internal Jugular Vein Anatomy, Common Carotid Artery Anatomy

    Ultrasound Mapping of the Anatomical Relationship Between the Right Internal Jugular Vein and Carotid Artery

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    This prospective observational study will describe the anatomical relationship between two major blood vessels on the right side of the neck: the internal jugular vein and the common carotid artery.

    Conditions
    Internal Jugular Vein Anatomy, Common Carotid Artery Anatomy, Cardiac Surgery
    Trial name
    IJVCCA (NCT07893080)
    Testing
    Standardized Ultrasound Imaging and Computer-Assisted Angular Mapping
    Where
    Turkey (Türkiye)
    Volunteers
    200 people
    Sponsor
    Ankara City Hospital Bilkent
    Can I take part? IJVCCA
  • Postoperative Cognitive Complications, Delirium

    Prospective Observational Multimodal Neuromonitoring During High-Risk Adult Surgery

    • Not yet recruiting
    • Age: 18 years and older
    • Observational study

    This is a prospective observational cohort study of adult patients undergoing high-risk surgery at UT Southwestern Medical Center.

    Conditions
    Postoperative Cognitive Complications, Delirium, Perioperative/Postoperative Complications, Brain Injuries
    Trial name
    NCT07577726
    Where
    United States
    Volunteers
    300 people
    Sponsor
    University of Texas Southwestern Medical Center
    Can I take part? NCT07577726
  • Right Ventricular Function, Prone Position

    Bedside Assessment of Right Ventricular Output Lying in Prone Or Supine

    • Not yet recruiting
    • Age: 18 years and older
    • Surgery or procedure

    Right ventricular failure (RVF) is a common complication to cardiac surgery, which is associated to mortality, kidney failure, stroke, prolonged mechanical ventilation and ICU stay.

    Conditions
    Right Ventricular Function, Prone Position, Atelectasis, Atelectases, Postoperative Pulmonary
    Trial name
    BAROLO (NCT07632027)
    Testing
    Prone position
    Where
    Sweden
    Volunteers
    70 people
    Sponsor
    Sahlgrenska University Hospital
    Can I take part? BAROLO
  • Atrial Fibrillation, Postoperative Atrial Fibrillation

    SGB for Prevention of Postop A-Fib After Cardiac SurgeryTrial

    • Not yet recruiting
    • Age: 18 years and older
    • Phase 3
    • Injection or infusion

    This research study is being conducted to determine whether a stellate ganglion block, a small injection in the neck that temporarily reduces sympathetic nervous system activity, can help reduce the risk of developing…

    Trial name
    NCT07893275
    Testing
    Stellate Ganglion Block Injection with 10 mL 0.5% Bupivacaine, Stellate Ganglion Block Injection with 10 mL Normal Saline
    Volunteers
    60 people
    Sponsor
    The Cleveland Clinic
    Can I take part? NCT07893275

Completed, with results posted

All 363
  • Hemorrhage, Surgical, Blood Loss, Surgical

    Safe and Timely Antithrombotic Removal - Ticagrelor (STAR-T)

    • Completed
    • Age: 18 years and older
    • Medical device
    • Results posted

    Prospective, multi-center, double-blind, randomized pivotal trial to evaluate the safety and effectiveness of the DrugSorb-Antithrombotic Removal (ATR) system for intraoperative removal of ticagrelor in patients undergoing urgent…

    Conditions
    Hemorrhage, Surgical, Blood Loss, Surgical, Blood Loss, Postoperative, Hemorrhage Postoperative
    Trial name
    STAR-T (NCT04976530)
    Testing
    DrugSorb-ATR system
    Where
    29 sites in United States, Canada
    Volunteers
    140 people
    Sponsor
    CytoSorbents, Inc
    Can I take part? STAR-T
  • Atrial Fibrillation, Atrial Flutter

    Colchicine For The Prevention Of Perioperative Atrial Fibrillation In Patients Undergoing Thoracic Surgery (COP-AF)

    • Completed
    • Age: 55 years and older
    • Phase 3
    • Results posted

    The prevention of perioperative atrial fibrillation (AF) and myocardial injury after non-cardiac surgery (MINS) has the potential to reduce mortality, stroke, and hospital stays in patients undergoing major thoracic surgery.

    Conditions
    Atrial Fibrillation, Atrial Flutter, Myocardial Injury After Non-Cardiac Surgery
    Trial name
    COP-AF (NCT03310125)
    Testing
    Active Colchicine
    Where
    46 sites in United States, Austria and 9 more
    Volunteers
    3,209 people
    Sponsor
    Population Health Research Institute
    Can I take part? COP-AF
  • Acute Kidney Injury

    Preop Digifab in CABG to Reduce Ouabain Levels and Prevent AKI

    • Completed
    • Age: 18 years and older
    • Phase 4
    • Results posted

    Acute kidney injury (AKI) occurs in up to 30% of patients undergoing coronary artery bypass graft (CABG) surgery, and often requires patients to go on dialysis.

    Trial name
    NCT03810417
    Testing
    Digoxin Antibodies Fab Fragments, Baseline EO > 360 pM, EO < 360 pM
    Where
    2 sites in United States
    Volunteers
    267 people
    Sponsor
    University of Maryland, Baltimore
  • Acute Kidney Injury

    Deferoxamine for the Prevention of Cardiac Surgery-Associated Acute Kidney Injury

    • Completed
    • Age: 18 years and older
    • Phase 2
    • Results posted

    Multiple lines of evidence support a central role of iron in causing acute kidney injury (AKI), including the finding that prophylactic administration of iron chelators attenuates AKI in animal models.

    Trial name
    DEFEAT-AKI (NCT04633889)
    Testing
    Deferoxamine, Normal saline
    Where
    3 sites in United States
    Volunteers
    320 people
    Sponsor
    Brigham and Women's Hospital
    Can I take part? DEFEAT-AKI
  • Open Heart Surgery

    Ilofotase Alfa for Prevention of Renal Damage After Cardiac Surgery

    • Completed
    • Age: 18 years and older
    • Phase 2
    • Results posted

    The aim of this clinical trial is to evaluate the efficacy and safety of two intravenous administrations of ilofotase alfa in patients at risk for renal damage following open heart surgery.

    Trial name
    NCT06168799
    Testing
    Ilofotase alfa
    Where
    13 sites in Belgium, Germany and 3 more
    Volunteers
    271 people
    Sponsor
    AM-Pharma
    Can I take part? NCT06168799

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