Cardiac Surgery Recovery

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

Condition / disease
Location
Status: Not yet recruiting

Older Adults' Recovery Dynamics After Cardiac Surgery

Population aging has increased the number of older adults exposed to interventions with high physiological demand, which are associated with frequent adverse outcomes such as delirium, organ dysfunction, and delayed functional recovery. Current clinical tools, such as frailty assessments, help identify higher-risk populations but do not adequately explain the marked individual variability in recovery or accurately predict who will develop complications. This variability may be partly explained by individual resilience, defined as the ability to recover toward, return to, or even surpass a prior functional state after an acute stressor. Evidence suggests that biological mechanisms related to aging influence resilience; however, biomarkers and integrated clinical models capable of characterizing and potentially modulating resilience in humans remain limited. Therefore, a standardized clinical platform is needed to characterize physiological resilience and its determinants, generating actionable knowledge to improve risk stratification, guide interventions, and optimize recovery in older adults. To this end, a single-center prospective cohort study will be conducted at Clinica Bicentenario Santiago, including individuals aged ≥65 years who are independent or have mild dependency and are undergoing elective cardiac surgery requiring sternotomy for valvular and/or coronary artery disease, recruited between 2026 and 2027. Participants will undergo a baseline assessment 2-3 weeks before surgery; an early postoperative assessment focused on the systematic recording of clinical outcomes, including delirium and organ dysfunction; and longitudinal follow-up to characterize recovery after discharge. Follow-up assessments will include frailty, intrinsic capacity (the composite of an individual's physical and mental capacities across the cognitive, locomotor, psychological, vitality, and sensory domains), functional status, health-related quality of life, and perceived fatigability, according to the prespecified assessment schedule. In addition, blood samples will be collected at three time points (baseline, 24 hours postoperatively, and one month after surgery) to measure plasma levels of growth differentiation factor 15 (GDF-15), a biomarker associated with aging-related biological stress and systemic responses to tissue injury. It is projected that at least 75 participants will be recruited over a 12-month period, allowing characterization of baseline clinical and functional profiles, the frequency of postoperative complications and organ dysfunction, trajectories of recovery, and associations between baseline characteristics, biological markers, and subsequent recovery outcomes.

Participants needed: 75
Trial details
Age: 65+Biological sex: AllType: ObservationalSponsor: University of ChileUpdated: Aug 28, 2026Locations: 1Duration: 12 Months
Eligibility criteria

Older adults (≥ 65 años) undergoing elective cardiac surgery via median sternoto... [+1]

Emergency surgery for any indication [+3]

Status: Not yet recruiting

Bedside Assessment of Right Ventricular Output Lying in Prone Or Supine Position

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. The right ventricle is particularly vulnerable to an increased afterload. By increasing pulmonary vascular resistance (PVR), atelectasis might mitigate a negative effect on the right ventricle. Recruitment maneuvers have been shown to resolve atelectasis and improve hemodynamics by increasing cardiac output and lowering PVR. However these maneuvers transiently raise airway pressures, which in turn increases right ventricular afterload, a situation often poorly tolerated by patients with RVF. Prone position is used in patients with respiratory failure and has been shown to decrease mortality in patients with ARDS. Prone position decreases atelectasis and moves ventilation dorsally. In ARDS it also seems to mediate beneficial hemodynamic effects such as an increase in cardiac output and a decrease in PVR. The investigators hypothesis is that prone position early after cardiac surgery will increase cardiac output by recruitment of atelectasis and thereby decrease PVR.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Sahlgrenska University HospitalUpdated: Jun 8, 2026Locations: 1
Eligibility criteria

Scheduled for cardiac surgery using cardiopulmonary bypass

BMI >40 [+6]

Status: Not yet recruiting

Jafron Cytokine Adsorber During Pediatric Open-Heart Surgeries

This prospective single-center randomized controlled trial aims at evaluating the safety and feasibility of an hemoadsorption protocol using Jafron HA-60 during cardio-pulmonary bypass in 20 pediatric patients undergoing open-heart surgery.

Participants needed: 20
Trial details
Age: Up to 10Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire VaudoisUpdated: Feb 10, 2026Locations: 1
Eligibility criteria

Children ≤ 10 years old at study inclusion [+3]

Children having an indication to receive hemoadsorption during CPB for drugs rem... [+7]

Status: Not yet recruiting

Responsive Nature-Driven Imagery to Reduce Delirium After Cardiac Surgery

The goal of this clinical trial is to learn if a novel device (MindfulGarden) is beneficial in a population of patients undergoing cardiac surgery. The main questions it aims to answer are: Is a novel device (MindfulGarden) that uses responsive nature-driven imagery feasible in patients undergoing cardiac surgery? Will use of this device reduce the use of psychotropic medications, improve recovery experience, and improve delirium? Participants will receive routine post-operative management and standard delirium reduction measures. They will be randomized into two groups where one receives the novel device (MindfulGarden) and the other does not.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of British ColumbiaUpdated: Jul 3, 2025Locations: 1
Eligibility criteria

Planned open-heart cardiac surgery (e.g. coronary artery bypass grafting, valve... [+2]

Severe pre-existing cognitive impairment (Montreal Cognitive Assessment [MOCA6]<... [+3]