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NCT07161908Recruiting

Controlled Remote Monitoring and Optimization of Oxygen Therapy in Preterm Infants

Early Detection and Prevention of Health Complications in Preterm Infants - Controlled Remote Monitoring and Optimization of Oxygen Therapy

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

The project is a national, prospective, multicenter, interventional pilot project focused on controlled remote monitoring and optimization of oxygen therapy for premature infants in the Czech Republic. The primary aim of the project is to prepare, test, and develop a proposal for a national methodology for the care of preterm newborns. This will reduce health risks in premature infants and minimize the negative impacts on the overall development of the child and the family of the premature infant.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
70 (estimated)
First submitted
12 Aug 2025
Start date
25 Aug 2025
Primary completion date
30 Apr 2027
Lead sponsor
Institute of Health Information and Statistics of the Czech Republic
NCT number
NCT07161908

What you commit to

  • Study type: Interventional
  • Planned participants: 70
  • From 25 Aug 2025 to the primary completion date, 30 Apr 2027
  • 4 sites 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.

Prior treatment

  • insufficient therapy through long-term home oxygen therapy

Other illness

  • child diagnosed with conditions other than bronchopulmonary dysplasia (BPD) at high risk of long-term hypoxia - selected chronic cardiovascular, neurological, and muscular diseases, e.g., significant congenital heart defects, congenital central nervous system developmental disorders, genetic diseases associated with the risk of hypoventilation, central apneas, severe early obstructive sleep apnea
  • other chronic respiratory diseases besides BPD - e.g., cystic fibrosis, chronic aspiration

Other

  • unsigned consent for participation in the project and/or consent for the processing of personal data
  • tracheostomy

Who the study is looking for

  • infants born before 31+6 weeks gestation
  • signed consent for participation in the project and consent for the processing of personal data
  • diagnosed with bronchopulmonary dysplasia
  • type of pulmonary ventilation - low-flow nasal cannulas

Age in the registry: - to 36 weeks · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

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

SiteCityCountrySite status
České Budějovice Hospital
Coordinator of this site? Confirm its status
České BudějoviceCzechiaRecruiting
University Hospital Olomouc
Coordinator of this site? Confirm its status
OlomoucCzechiaRecruiting
General University Hospital
Coordinator of this site? Confirm its status
PragueCzechiaRecruiting
Institute for the Care of Mother and Child
Coordinator of this site? Confirm its status
PragueCzechiaRecruiting

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