Oral Ibuprofen Prophylaxis for Patent Ductus Arterioses in Very Extremely Low Birth Weight Infants
Information source: Zekai Tahir Burak Maternity and Teaching Hospital
Information obtained from ClinicalTrials.gov on February 07, 2013 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Oral Ibuprofen Prophylaxis in Very Low Birth Weight Infants
Intervention: ibuprofen (Drug); ibuprofen (Drug)
Phase: N/A
Status: Recruiting
Sponsored by: Zekai Tahir Burak Maternity and Teaching Hospital Overall contact: H. Gozde Kanmaz, MD, Phone: 90 505 588 11 89, Email: gzdekanmaz@yahoo.com
Summary
Patent ductus arterioses (PDA) is a major morbidity in preterm infants, especially in
extremely premature infants less than 28 weeks. The clinical signs and symptoms of PDA in
preterm infants are non specific and insensitive for making an early diagnosis of
significant ductal shunting. Functional echocardiography is emerging as a new valuable
bedside tool for early diagnosis of hemodynamically significant ductus, even though there
are no universally accepted criteria for grading the hemodynamic significance.
Echocardiography has also been used for early targeted treatment of ductus arterioses,
though the long term benefits of such strategy are debatable. The biomarkers like BNP and N-
terminal pro-BNP are currently under research as diagnostic marker of PDA. The primary mode
of treatment for PDA is pharmacological closure using cyclo-oxygenase inhibitors with
closure rate of 70-80%. Oral ibuprofen is emerging as a better alternative especially in
Indian scenario where parenteral preparations of indomethacin are unavailable and side
effects are comparatively lesser. Though pharmacological closure of PDA is an established
treatment modality, there is still lack of evidence for long term benefits of such therapy
as well as there is some evidence for the possible adverse effects like increased ROP and
BPD rates, especially if treated prophylactically. The aim of this study is to investigate
the effect of oral ibuprofen prophylaxis administrated on the first 24 hours of life and the
following two days on hemodynamically significant patent ductus arterioses and its long term
effects such as ROP and BPD.
Clinical Details
Official title: Oral Ibuprofen Prophylaxis for Patent Ductus Arterioses in Very Extremely Low Birth Weight Infants
Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention
Primary outcome: the effect of oral ibuprofen to prevent hemodynamically significant PDA (hs-PDA) and from rescue therapy
Secondary outcome: long term effects of oral ibuprofen prophylaxis in VELBW
Detailed description:
Patent ductus arterioses (PDA) is a major morbidity encountered in preterm neonates,
especially in babies less than 28 weeks gestation or 1000g. Natural ductal closure is
inversely related to gestational age and birth weight. The incidence ranges from 15% to 37%
in newborn babies less than 1750 grams. The presence of PDA has significant effects on
myocardial functions as well as systemic and pulmonary blood flow. Preterm newborns adapt,
by increasing the left ventricular contractility, and thereby maintaining the effective
systemic blood flow even when the left to right shunts equals 50% of the left ventricular
output. This is mainly accomplished by an increase in stroke volume (SV)rather than heart
rate. This increase in stroke volume is primarily due to reduction in afterload and
simultaneous increase in left ventricular preload. An increasing number of biological
substances like hormones, enzymes which are markers of cardiac stress, dysfunction or
myocardial injury-collectively called biomarkers-are emerging as diagnostic and prognostic
markers especially in the setting of heart failure or ischemic injury. The pharmacological
basis for medical therapy is the use of non selective cyclo-oxygenase (COX) inhibitors,
which inhibits prostaglandin synthesis and causes ductal constriction. The two most widely
studied and used non selective COX inhibitors are indomethacin and ibuprofen. The future of
pharmacological treatment of PDA could be with the use of nitric oxide inhibitors and
prostaglandin receptor antagonists. Ibuprofen is an effective choice for the treatment of
PDA in preterm infants as it has been demonstrated in previous several studies. Since there
is a meta-analysis that claims there is no need for further studies about ibuprofen
prophylaxis to treat PDA in low birth weight infants we aimed to evaluate the effect of
ibuprofen prophylaxis in very extremely low birth weight infants. One such marker emerging
in the diagnosis of hs-PDA is brain natriuretic peptide (BNP). Natriuretic peptides are
hormones, produced either by atria (atrial natriuretic peptide-ANP) or by ventricles (BNP)
in response to myocardial stress, secondary to dilatation, hypertrophy or increased wall
tension. One of the aims of this study is to investigate the effect of oral prophylactic
ibuprofen administration on BNP levels and renal functions.
Eligibility
Minimum age: 23 Weeks.
Maximum age: 28 Weeks.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- < 28 gestational week and/or < 1000 g birth weight preterm infants written parent
consent
Exclusion Criteria:
- major congenital anomalies
- congenital heart diseases
- not having written parent consent
Locations and Contacts
H. Gozde Kanmaz, MD, Phone: 90 505 588 11 89, Email: gzdekanmaz@yahoo.com
Zekai Tahir Burak Maternity Teaching Hospital, Ankara, Turkey; Recruiting H. Gozde Kanmaz, MD, Phone: 90 505 588 11 89, Email: gzdekanmaz@yahoo.com Omer Erdeve, MD, Email: omererdeve@yahoo.com
Additional Information
Related publications: Gokmen T, Erdeve O, Altug N, Oguz SS, Uras N, Dilmen U. Efficacy and safety of oral versus intravenous ibuprofen in very low birth weight preterm infants with patent ductus arteriosus. J Pediatr. 2011 Apr;158(4):549-554.e1. Epub 2010 Nov 20. Erdeve O, Gokmen T, Altug N, Dilmen U. Oral versus intravenous ibuprofen: which is better in closure of patent ductus arteriosus? Pediatrics. 2009 Apr;123(4):e763. No abstract available.
Starting date: July 2011
Last updated: July 21, 2011
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