Ductus Arteriosus, Patent

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Review clinical trials related to Ductus Arteriosus, Patent. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Percutaneous Intervention Versus Observational Trial of Arterial Ductus in Low Weight Infants

Patent Ductus Arteriosus is a developmental condition commonly observed among preterm infants. It is a condition where the opening between the two major blood vessels leading from the heart fail to close after birth. In the womb, the opening (ductus arteriosus) is the normal part of the circulatory system of the baby, but is expected to close at full term birth. If the opening is tiny, the condition can be self-limiting. If not, medications/surgery are options for treatment. There are two ways to treat patent ductus arteriosus - one is through closure of the opening with an FDA approved device called PICCOLO, the other is through supportive management (medications). No randomized controlled trials have been done previously to see if one of better than the other. Through our PIVOTAL study, the investigators aim to determine is one is indeed better than the other - if it is found that the percutaneous closure with PICCOLO is better, then it would immediately lead to a new standard of care. If not, then the investigators avoid an invasive costly procedure going forward.

Participants needed: 240
Trial details
Age: 7-32Biological sex: AllType: InterventionalSponsor: Nationwide Children's HospitalUpdated: Mar 30, 2025Locations: 24
Eligibility criteria

EPIs born between 22-weeks+0 days (220/7 wks) and 27-weeks+6 days (276/7 wks) ge... [+5]

Life-threatening congenital defects (including congenital heart disease such as... [+14]

Status: Not yet recruiting

The U.S. PDA Registry

The objective of this study is to demonstrate the continued safety and efficacy in a real-world setting of transcatheter device closure of the PDA in premature infants less than 2kg in weight at the time of device implant using the Amplatzer Piccolo Occluder device and other devices performed in the USA.

Participants needed: 5,000
Trial details
Age: 3-1Biological sex: AllType: ObservationalSponsor: Le Bonheur Children's HospitalUpdated: Dec 20, 2019Locations: 1
Eligibility criteria

Diagnosis of PDA. [+2]

Weight <700 gm or greater than or equal to 2 kg at the time of device implant. [+6]