Pulmonary Hypertension Trial, Recruiting NCT07161908 Sponsor: Institute of Health Information and Statistics of the Czech Republic Condition: Pulmonary Hypertension
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Pulmonary Hypertension Trial, Recruiting

NCT07161908
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Your baby was born before 32 weeks of pregnancy (premature birth)
  • A parent or guardian has signed the consent forms to take part in the study and to allow personal data to be used
  • Your baby has been diagnosed with a lung condition called bronchopulmonary dysplasia (BPD), which is a chronic lung disease that can develop in premature babies
  • Your baby is currently receiving oxygen through low-flow nasal cannulas (small tubes that sit just inside the nostrils and deliver a gentle flow of oxygen)

Who may not be able to join:

  • A parent or guardian has not signed the required consent forms for participation or for personal data use
  • Your baby has been diagnosed with other serious long-term conditions beyond BPD that could cause low oxygen levels, such as significant heart defects present at birth, developmental disorders of the brain or nervous system, genetic conditions linked to breathing problems, central apneas (pauses in breathing controlled by the brain), or severe obstructive sleep apnea
  • Your baby has another long-term lung or breathing condition in addition to BPD, such as cystic fibrosis or ongoing problems caused by repeatedly inhaling fluids (chronic aspiration)
  • Your baby's current long-term home oxygen therapy is not working well enough to manage their condition (confirm with trial site)
  • Your baby has a tracheostomy (a surgical opening in the throat used for breathing)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 21 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Richard Plavka, prof., General Hospital University in Prague

Phone: +420725441408

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Institute of Health Information and Statistics of the Czech Republic
Registry
ClinicalTrials.gov
Start date
25 August 2025
Est. completion
1 November 2026

Where this trial is recruiting

🇨🇿 Czechia

Primary endpoints

Average duration of controlled oxygen therapy in a premature infant

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov