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NCT07785141Recruiting

Spectroscopic Assessment of Myocardial Oxygenation Changes in Pediatric Heart Surgery

Source: ClinicalTrials.gov · Last updated 28 Sept 2026

Brief summary (registry, in English)

The goal of this observational study is to investigate the ability of the SpectroCor Tissue Oxygenation Monitor and its accessory SpectroCor Sensor to observe and monitor changes in cardiac oxygen availability in pediatric patients during open-heart surgery. Patients of less than 18 years old who, and whose guardian(s), when applicable according to national legislation, have signed the informed consent, can participate in the study. The primary hypothesis is that the SpectroCor Tissue Oxygenation Monitor and its accessory SpectroCor Sensor can detect myocardial oxygen availability in pediatric open-heart surgery patients. It is expected that the detected tissue oxygenation timely correlates with procedures affecting myocardial perfusion and other clinical parameters during the operation. The secondary hypothesis is that the SpectroCor Tissue Oxygenation Monitor and its accessory, the SpectroCor Sensor, are safe to use, and their usability is acceptable. No comparison group is included in the study. The devices are used by the study investigators during open-heart surgery to collect myocardial tissue spectrometer data from the pediatric population to validate and potentially further develop the monitor and its accessory, the sterile sensor. The follow-up period for each participant ends with discharge from the hospital. No data (such as questionnaires) are obtained directly from the study participants.

Status (registry)
Recruiting
Study type
Observational
Enrollment
30 (estimated)
First submitted
20 Aug 2026
Start date
17 Sept 2026
Primary completion date
31 Dec 2027
Lead sponsor
Spectrocor
NCT number
NCT07785141

What you commit to

  • Study type: Observational
  • Planned participants: 30
  • From 17 Sept 2026 to the primary completion date, 31 Dec 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Inability to provide informed consent

Who the study is looking for

  • Scheduled for open-heart surgery.
  • Age \<18
  • Signed informed consent

Age in the registry: 1 year to 17 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
HUS New Childrens Hospital
Coordinator of this site? Confirm its status
HelsinkiFinlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.