Pulmonary Hypertension Trial, Recruiting NCT07099144 Sponsor: Lee's Pharmaceutical Limited Condition: Pulmonary Hypertension
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Pulmonary Hypertension Trial, Recruiting

NCT07099144
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 at 34 weeks of pregnancy or later
  • Your baby has breathing problems caused by low oxygen levels that have needed breathing machine support for more than 24 hours
  • Your baby has signs of high blood pressure in the lungs, either from a clinical assessment or from a heart ultrasound (echocardiogram) showing specific measurements (confirm with trial site)
  • Your baby is less than 7 days old when the study treatment would begin
  • You (as the baby's guardian) agree to take part and sign a consent form

Who may not be able to join:

  • Your baby's body depends on a specific abnormal blood flow pattern to survive (confirm with trial site)
  • Your baby's mother received blood-thinning medications during pregnancy
  • Your baby's heart ultrasound shows a particular type of abnormal blood flow or a weakened left side of the heart (confirm with trial site)
  • Your baby urgently needs, or has already received, a special life-support machine called ECMO
  • Your baby is expected to pass away within the next 24 hours
  • Your baby has a serious life-threatening physical abnormality affecting the head, heart, or chest
  • Your baby has a chromosomal condition (such as Down syndrome or similar)
  • Your baby was born with a hole in the diaphragm (the muscle separating the chest and belly)
  • Your baby has a heart defect present from birth (apart from certain minor, common ones)
  • Your baby needed chest compressions during resuscitation within 6 hours before the study treatment would start
  • Your baby has serious bleeding problems, such as severe brain bleeding or uncontrolled bleeding
  • Your baby has a blood-clotting disorder called disseminated intravascular coagulopathy
  • Your baby is having active seizures while already receiving anti-seizure medication
  • Your baby experienced a prolonged lack of oxygen with signs of severe acid buildup in the blood
  • Your baby is currently receiving certain medications that release nitric oxide, such as prilocaine, sodium nitroprusside, nitroglycerin, or sulfonamides
  • The trial doctor decides for any other reason that your baby is not suitable for the study

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 27 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

Phone: +86-18017591123

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
Lee's Pharmaceutical Limited
Registry
ClinicalTrials.gov
Start date
12 December 2024
Est. completion
31 December 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

To evaluate the safety of inhaled nitric oxide combined with ventilatory support in the treatment of neonatal (≥ 34 weeks gestational age) hypoxic respiratory failure with pulmonary hypertension.

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: 27 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