Blood Based Assessment of sST2, Taken During and After Surgery, for Pediatric Patients With Heart Defects to Predict Heart Failure.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 18
SponsorMartin Schweiger

About this trial

Patients younger than 18 scheduled for congenital heart surgery will be assessed during and post-operatively as well as at the first follow-up after 9-12 month for the novel biomarker sST2. We will assess the marker independently and in evaluation with other blood biomarkers to evaluate sings of heart failure. Compared to established biomarkers, sST2 promises thereby to be less variable to factors like age or acute kidney injury, rendering it potentially more reliable in the field of congenital cardiac surgery.

Eligibility criteria

Qualifiers

Consented for cardiopulmonary bypass surgery for cardiac reason

Conversational skills in German (by child and/or representative) to be able to fully understand and sign a written consent in German language

Disqualifiers

Know genetic life limiting conditions

Syndrome patients who are scheduled or highly likely to be operated on more than one organ

Body weight at time of surgery less than 2.5 kg

Being recruited and enrolled for an interventional study protocol

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

225 Participants
are grouped into 1 trial group

Sponsors and collaborators

Martin Schweiger

Lead sponsor

University Children's Hospital, Zurich

Sponsor institution

University Children's Hospital, Zurich

Collaborator