Cardiovascular Surgery

11

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

Condition / disease
Location
Status: Recruiting

Appropriateness of Hemostatic Agent Use in Cardiovascular Surgery (HAEMOVAX)

Hemostatic agents are widely used in cardiac and vascular surgery to support intraoperative bleeding control. Despite their clinical relevance and substantial economic impact, little is known about real-world patterns of use, adherence to evidence-based recommendations, and the alignment between clinicians' perceived knowledge and actual decision-making. HAEMOVAX is a single-center mixed-methods observational study conducted at IRCCS Galeazzi-Sant'Ambrogio Hospital, Milan, Italy. The study combines an anonymous survey of cardiovascular surgeons with a retrospective audit of institutional hemostatic agent consumption. The primary objective is to evaluate the appropriateness of hemostatic agent selection using a Knowledge-Practice Alignment Score (KPA-Score) derived from standardized clinical vignettes based on current EACTS and ESA recommendations. Secondary objectives include assessment of usage patterns, barriers to appropriate use, concordance between declared practice and real-world consumption, and opportunities for evidence-based standardization.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: University of MilanUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

Physicians with a surgical role in the Departments of Cardiac Surgery or Vascula... [+2]

Non-surgical healthcare personnel (e.g., nurses, anesthesiologists, administrati... [+4]

Status: Recruiting

The Effects of a 6-week Pre-operative Administration of a Microbiome Modulator "WellBiome" Versus Placebo on Cardiac Surgical Outcomes and NHS Cost Savings.

More than 7.4 million people in the UK are currently waiting for surgery. Behind that number are real people-patients preparing mentally and physically for procedures ranging from joint replacements to major heart and abdominal operations. This research forms part of a broader strategy known as prehabilitation - preparing the body before surgery to improve outcomes afterward. For patients waiting for surgery, it represents a shift from passive waiting to active preparation. Heart surgery for bypass or valve replacements results in inevitable yet controlled trauma. It increases inflammation, stress hormones and immune system demand. The body then has to repair itself - quickly and efficiently. And here's the surprising part. Inside your gut live trillions of bacteria - called your gut microbiome. These bacteria help regulate inflammation, strengthen your immune system and protect against infection. This randomised clinical trial is investigating a fascinating question: Can improving your gut microbiome through consumption of fibre before surgery help you recover faster, reduce time in ICU, shorten hospital stays, and lower complication rates? The placebo controlled trial will randomise 80 patients following eligibiilty checks to either 5g of prebiotic fibre/300mg of magnesium (WellBiome) OR 5g of maltodextrin for a period of 6-8 weeks prior to surgery. Patient will provide blood, urine and faecal samples at baseline and upon admission for surgery, and two further blood samples at day 3 and 6 post operatively. Following surgery, patient outcomes will be assessed and compared between the experimental group (prebiotic fibre/magnesium) and placebo group (maltodextrin). The investigators are focussing on the time spent in the intensive care unit, complications and overall hospital stay. By documenting and quantifying these the investigators can calculate the costs and any savings between the groups.

Participants needed: 80
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: Hull University Teaching Hospitals NHS TrustUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

Aged 50-80 [+6]

Active cancer [+6]

Status: Recruiting

Fascial Plane Blocks In Cardiac Surgery

The aim of the present study is to evaluate the effects of the recto-intercostal fascial plane block (RIFPB) or the rectus sheath block (RSB) combined with the pectoral-intercostal fascial plane block (PIFPB) on postoperative analgesia in patients undergoing cardiac surgery.

Participants needed: 90
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Antalya Health Sciences UniversityUpdated: Jun 3, 2026Locations: 1
Eligibility criteria

elective cardiac surgery planned [+2]

under 18 years of age, [+9]

Status: Recruiting

Nutritional Effects in Cardiovascular Surgery

This study aims to investigate the distribution of gut microbiota-derived metabolites, and to evaluate whether postoperative nutritional intervention can modulate the gut-heart metabolic axis, thereby improving metabolic profiles and clinical outcomes.

Participants needed: 30
Trial details
Age: 50-80Biological sex: AllType: InterventionalSponsor: Fu Jen Catholic UniversityUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Scheduled to undergo cardiovascular surgery [+3]

Use of antibiotics, probiotics, or other treatments affecting gut microbiota wit... [+1]

Status: Not yet recruiting

Cardiovascular Surgery Early Prediction System for AKI :CARDS-AKI Registry

This multicenter, prospective study prospectively enrolled patients undergoing cardiovascular surgery. Detailed perioperative clinical data and biospecimens were collected at multiple time points. The primary aim is to develop an early warning model for postoperative acute kidney injury (AKI) by integrating clinical data and biomarkers. Additionally, through long-term follow-up, the study seeks to characterize outcome trajectories and establish a prognostic model for AKI patients. This study addresses four key questions: 1) Integration of clinical information and biomarkers to develop an early predictive model for cardiac surgery-associated acute kidney injury (CSA-AKI); 2) Identification of risk factors for CSA-AKI occurrence; 3) Determinants of prognosis in patients with CSA-AKI; and 4) Enhanced prediction of near- and long-term clinical event risks in this patient population. Participants will receive standard perioperative management. The study protocol includes the following procedures:(1) Clinical Data Collection: Comprehensive perioperative clinical data will be systematically recorded. (2) Biospecimen Sampling: Serial blood and urine samples will be obtained at predefined time points throughout the perioperative period. (3) In-Hospital Monitoring: Clinical outcomes will be continuously monitored during the hospital stay. (3) Post-discharge Follow-up: Participants will be assessed at regular intervals after discharge to track the occurrence of major adverse events. These findings provide a foundational basis for the development of a data-driven early-warning system. Such a system is designed to facilitate the prompt identification of high-risk patients and enable the initiation of personalized treatment strategies, thereby potentially improving clinical outcomes and optimizing resource allocation

Participants needed: 5,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Chinese Academy of Medical Sciences, Fuwai HospitalUpdated: Jan 9, 2026Locations: 1Duration: 2 Years
Eligibility criteria

Age ≥ 18 years; [+2]

Preoperative serum creatinine > 353 μmol/L, history of or currently receiving di... [+2]

Status: Recruiting

AI Model for Assessing Cardiac Surgeons' Techniques

The goal of this study aims to investigate the use of artificial intelligence to analyze and evaluate the characteristics and proficiency of surgeons during vascular anastomosis in coronary artery bypass grafting (CABG) procedures. The main question it aims to answer is: Consistency assessment between AI evaluation scores and human expert evaluation scores for surgeons during left anterior descending (LAD) artery anastomosis.

Participants needed: 284
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: China National Center for Cardiovascular DiseasesUpdated: Sep 23, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years [+3]

Patients with acute coronary syndrome [+2]

Status: Recruiting

Exploring the Predictive Value of Electroencephalography Features in Perioperative Neurocognitive Disorders Following Cardiovascular Surgery

To explore the predictive value of Electroencephalography features in Perioperative Neurocognitive Disorders in patients undergoing cardiovascular surgery under general anesthesia

Participants needed: 100
Trial details
Age: 60+Biological sex: AllType: ObservationalSponsor: Beijing Chao Yang HospitalUpdated: May 30, 2025Locations: 1
Eligibility criteria

Written informed consent [+4]

history of severe neurological diseases and psychiatric diseases [+6]

Status: Not yet recruiting

Protective Effect of Angong Niuhuang Against Negative Inflammatory Response and Neurologic Dysfunction After Cardiovascular Surgery

Neurologic Dysfunction is one of the main factors contributing to poor outcomes in cardiac surgery patients, except for heart failure. Atherosclerosis of the aorta, a history of cerebral infarction, and cervical artery disease are common clinical risk factors for cerebral neurological dysfunction after cardiac surgery. Results of preclinical studies suggested that Angong Niuhuang Pills (ANPs), a traditional Chinese patent medicine, including realgar, cinnabaris, Bovis Calculus, artificial Moschus, and powdered buffalo horn extract, decreased infarct volume and cerebral edema, and presented anti- atherosclerosis and cardio-protective effects in clinical and preclinical studies. The PANDA X trial is designed as a pilot study to explore the safety and efficacy of ANP in patients with moderate-to-severe neurologic dysfunction after cardiovascular surgery.

Participants needed: 120
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Nanjing Medical UniversityUpdated: Dec 12, 2024Locations: 2
Eligibility criteria

(1) an age > 18 years, [+5]

(1) not suitable for taking ANP after the dialectical process by a traditional C... [+3]

Status: Not yet recruiting

Development of Perioperative Delirium Prediction Model

Postoperative delirium is an acute organic brain dysfunction that is commonly observed following cardiovascular surgery. It presents with acute and fluctuating changes in the level of consciousness, resulting in impaired cognitive function and perception. The incidence of delirium following cardiac surgery has been reported to range from 11.4% to 55%. In light of the challenges associated with treating delirium once it has manifested, it is imperative to prioritise the early recognition and prevention of this condition. The objective of this study was to develop a perioperative delirium risk prediction model for patients undergoing cardiovascular surgery.

Participants needed: 770
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Kubra GunesUpdated: Nov 12, 2024Duration: 3 Days
Eligibility criteria

Over 18 years old [+4]

Cardiovascular surgery under emergency conditions [+5]

Status: Recruiting

Effectiveness of a Intraoperative Blood Recovery System in Cardiovascular Surgery in Brazil

Randomized trial to evaluate the effectiveness of a intra operative blood recovery system in reducing the need for allogeneic transfusion in cardiovascular surgeries using cardiopulmonary bypass

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Instituto Materno Infantil Prof. Fernando FigueiraUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

all patients undergoing CABG or Valve surgery singly.

Emergency cardiac surgery; [+6]

Status: Recruiting

Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry

The Accuryn Registry Study is an open-ended, global, multi-center, retrospective and prospective, single-arm data collection study with an FDA cleared device. The target population are cardiovascular surgery patients. Physiologic data measurements will be collected from enrolled subjects using electronic medical records and data streams via the Accuryn Monitoring System.

Participants needed: 2,500
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Potrero MedicalUpdated: Sep 28, 2022Locations: 9
Eligibility criteria

Signed or Verbal Informed Consent as required by IRB (if applicable). [+3]

Known history of advanced chronic kidney disease defined by an estimated glomeru... [+1]