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Clinical Trials/NCT04062396
NCT04062396CompletedNot Applicable

Randomized Comparison Between Oxygenator Systems for the Reduction of Post-operative Delirium in Older Patients Undergoing Cardiac Surgery

Maria Cecilia Hospital2 sites in 1 country154 target enrollmentStarted: September 26, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
154
Locations
2
Primary Endpoint
post-operative delirium

Study Overview

Brief Summary

Age is no longer an absolute contraindication to cardiac surgery therefore there is often need for combined interventions (double valve repair/replacement, or coronary artery bypass graft and valve repair/replacement) with relative prolongation of cardiopulmonary bypass time. Prolonged cardiopulmonary bypass use causes an increase in the inflammatory response, and on the other a need for blood reinfusion and therefore lipid microemboli from the operative field. The clinical consequences for patients are post-operative delirium and post-operative cognitive impairment.

These two neurological complications involve up to 45% of elderly patients undergoing cardiac surgery and have a significant impact on quality of life, hospitalization and mortality in the short and long term. The Remowell 2 oxygenator system has demonstrated in preliminary studies that, compared to the gold standard Inspire oxygenator, it can guarantee a significant reduction of hemodilution, inflammatory systemic response and embolization of lipid microemboli and leukocytes. In light of these considerations, it is possible to formulate the hypothesis that the use of the Remowell 2 device can contribute to significantly reducing the onset of post-operative delirium and cognitive impairment. The present study is designed to validate this hypothesis in a randomized controlled scenario.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
65 Years to — (Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Signature of informed consent for participation in the study
  • Age ≥65 years
  • Patients undergoing cardiac surgery of:
  • coronary artery bypass graft and concomitant valve replacement/repair OR
  • double valve replacement/repair

Exclusion Criteria

  • Any documented history of cognitive impairment estimated as a mini mental state examination < 24 points
  • Patients who need blood prime in the cardiopulmonary bypass circuit
  • Chronic coagulopathies ( international normalized ratio > 2 in patients without anticoagulant treatment)
  • End stage renal disease on dialysis treatment
  • Previous cerebrovascular accident
  • Active cancer or immunological diseases
  • Liver cirrhosis (platelets <100.000/uL)
  • Decompensated diabetes
  • Severe preoperative anemia (hemoglobin <8 g/dl).

Outcomes

Primary Outcomes

post-operative delirium

Time Frame: 6 days

In-hospital incidence of post-operative delirium assessed by Confusion Assessment Method (CAM) diagnostic algorithm

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Maria Cecilia Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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