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Second Course of Therapy for Resistant Patent Ductus Arteriosus (PDA)

S

Shaare Zedek Medical Center

Status and phase

Withdrawn
Phase 2

Conditions

Patent Ductus Arteriosus

Treatments

Drug: Indomethacin
Drug: Ibuprofen

Study type

Interventional

Funder types

Other

Identifiers

NCT01070745
chammerman3

Details and patient eligibility

About

Patency of the ductus arteriosus (PDA) is functionally essential for fetal circulation, however persistence of ductal patency postnatally may have significant adverse hemodynamic effects in the neonate. Medical therapy for PDA predominantly involves the administration of one of two non-steroidal anti-inflammatory drugs: indomethacin or ibuprofen. Both of these therapies have been shown to be successful in mediating ductal closure in approximately 70% of treated infants.

However, the need for a second course of treatment for PDA closure remains quite common. The investigators hypothesize that, because of small differences between the two drugs, a greater percentage of infants who did not respond to a first course of therapy with indomethacin will respond to a second course with ibuprofen than to a repeat course of indomethacin.

As such, the investigators aim to compare secondary therapy with a repeat course of indomethacin to secondary therapy with ibuprofen in infants whose ductus remained patent after a first course of therapy with indomethacin.

Sex

All

Ages

2 days to 2 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Inborn premature neonates (birth weight [BW] <1500 grams) being treated in the neonatal intensive care unit of the Shaare Zedek Medical Center and diagnosed as still having a hemodynamically significant patent ductus arteriosus (hsPDA) after a first course of therapy with indomethacin, will be considered as potential candidates for study pending response to initial therapy and pending parental consent.

Exclusion criteria

  • Any baby not considered viable
  • Any baby with intraventricular hemorrhage (IVH) grade 3-4 of recent onset (within 3 days). [If no head ultrasound has been performed within the last 3-4 days, one should be performed prior to onset of study.]
  • Any baby with dysmorphic features or congenital abnormalities
  • Any baby with structural heart disease other than PDA
  • Any baby with documented infection,
  • Any baby with thrombocytopenia (<50,000).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

0 participants in 2 patient groups

Indomethacin for resistant PDA
Experimental group
Description:
Treatment with second course of indomethacin
Treatment:
Drug: Indomethacin
Ibuprofen for resistant PDA
Experimental group
Description:
Ibuprofen as second course of therapy
Treatment:
Drug: Ibuprofen

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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