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Patent Ductus Arteriosus clinical trials

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NCT ID: NCT01758913 Completed - Clinical trials for Patent Ductus Arteriosus

Closure of Patent Ductus Arteriosus With Indomethacin or Ibuprofen in Extreme Low Birth Weight Infants

Start date: February 2007
Phase: N/A
Study type: Interventional

Pharmacological closure of ductus arteriosus with prostaglandin (PG) inhibitors has been used for years. Previous studies indicated that ibuprofen has similar effect on ductal closure as indomethacin but has less adverse effects on renal function, cerebral blood flow and mesenteric blood flow.1-7 There are, however, very few studies being done specifically on extremely low birth weight (ELBW) infant < 1000 g. This group of infants has immature kidney and often has poor response to PG inhibitors and has high mortality and morbidity. We hypothesized that, in ELBW infants, the ductal and renal response to PG inhibitors may be different between indomethacin and ibuprofen.

NCT ID: NCT01630278 Completed - Clinical trials for Patent Ductus Arteriosus

Early Ibuprofen Treatment of Patent Ductus Arteriosus (PDA) in Premature Infants (TRIOCAPI)

TRIOCAPI
Start date: March 2012
Phase: Phase 3
Study type: Interventional

Very premature infants with a large ductus, selected by an early echocardiogram, will receive either ibuprofen or placebo before 12 hours of life. Follow-up will include repeated echocardiograms and cranial ultrasound at 36 hours, 14 days and 36 weeks of postconceptional age. The primary outcome will be survival without cerebral palsy at years.

NCT ID: NCT01593163 Completed - Clinical trials for Patent Ductus Arteriosus

Echocardiographically Guided Versus Standard Ibuprofen Treatment for Patent Ductus Arteriosus

Start date: May 2009
Phase: Phase 3
Study type: Interventional

Patent ductus arteriosus (PDA) is a very common condition in immature newborn babies and it has been associated to morbidity and mortality. Ibuprofen is the drug of choice for PDA treatment according to the last version of the Cochrane review. Nowadays the best dose regimen for ibuprofen remains uncertain. The investigators aim to perform a randomized controlled clinical trial to assess whether echocardiographically guided PDA ibuprofen treatment versus standard treatment could reduce the number of doses of ibuprofen without increasing the reopening rate and reducing the side effects associated to this medication.

NCT ID: NCT01536158 Completed - Clinical trials for Patent Ductus Arteriosus

Oral Paracetamol Versus Oral Ibuprofen in Management of Patent Ductus Arteriosus in Preterm Infants: A Randomised Controlled Trial

Start date: February 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine whether oral paracetamol or ibuprofen has a better or same efficacy and tolerance in closure of patent ductus arteriosus in preterm infants.

NCT ID: NCT01511887 Completed - Clinical trials for Patent Ductus Arteriosus

Safety and Efficacy of Ibuprofen in Term Newborns With Patent Ductus Arteriosus (PDA)

Start date: January 2011
Phase: N/A
Study type: Interventional

The aim of current study is to evaluate the efficacy and safety of oral Ibuprofen in term 20-28 days old newborn referred to Bandarabbas children' hospital in 2011.

NCT ID: NCT01497054 Completed - Clinical trials for Patent Ductus Arteriosus

Do Elevated BNP Levels Predict Hemodynamically Significant PDAs

Start date: December 2011
Phase: N/A
Study type: Observational

The purpose of this study is to determine if B type natriuretic peptide (BNP) levels can be used to predict a hemodynamically significant patent ductus arteriosus (PDA). This peptide is produced by the ventricles in the heart when they are under stress, such as when a ductus remains open. If we can use a simple and inexpensive blood test to determine whether a PDA needs to be treated, we can potentially treat infants sooner than if they needed to wait for the availability of a cardiologist to perform an echocardiogram. This might decrease some of the deleterious effects of PDAs on the preterm infant such as bronchopulmonary dysplasia, necrotizing enterocolitis, renal hypoperfusion, and pulmonary hemorrhage. In a situation where follow up echocardiogram after a course of medical therapy shows persistent PDA, this test may help to decide whether this baby needs further treatment, either medical or surgical.

NCT ID: NCT01479218 Completed - Clinical trials for Patent Ductus Arteriosus

Safety and Effectiveness Study With a New PDA Occluder for Closure of Patent Ductus Arteriosus

Start date: November 2011
Phase: N/A
Study type: Interventional

The objective of the study is to investigate the safety, efficacy and clinical utility of the Occlutech PDA device for closure of patent ductus arteriosus of all types.

NCT ID: NCT01428180 Completed - Clinical trials for Patent Ductus Arteriosus

Influence of Treatment for Patent Ductus Arteriosus on Cerebral Oxygenation in Preterm Infants

Start date: April 2011
Phase: Phase 4
Study type: Observational

The purpose of this study is to examine the influence medical or surgical treatment for patent ductus arteriosus in preterm infants on cerebral and renal tissue oxygenation and on cardiac output.

NCT ID: NCT01261117 Completed - Clinical trials for Patent Ductus Arteriosus

Efficacy and Safety of Oral Versus Intravenous Ibuprofen for PDA Treatment in ELBW Infants

Start date: January 2009
Phase: N/A
Study type: Interventional

To determine whether oral or intravenous ibuprofen has a better or same efficacy and tolerance in closure of patent ductus arteriosis in extremely-low-birth-weight preterm infants.

NCT ID: NCT00795990 Completed - Clinical trials for Patent Ductus Arteriosus

Timing for the Medical Treatment of Patent Ductus Arteriosus in Preterm Infants

Start date: November 2008
Phase: N/A
Study type: Observational

This is a retrospective chart review to look at the timing of using indomethacin and ibuprofen for PDA closure for infants admitted into the NICU of the University of Utah Hospital from 1/2007-8/2008. The purpose is to compare the outcomes of medical intervention in preterm infants if intervention occurs day of life 4 or less, or day of life 5 or greater, with the birthdate being counted as day of life 1.