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| Sponsor: | University of Virginia |
|---|---|
| Information provided by: | University of Virginia |
| ClinicalTrials.gov Identifier: | NCT00500305 |
Purpose
A patent ductus arteriosus (PDA) is associated with increased morbidity in premature infants. Standard indomethacin treatment is associated with intestinal and renal morbidity. B-type natriuretic peptide is elevated in significant PDAs. This study will determine whether BNP guided therapy could reduce doses of indomethacin.
| Condition | Intervention |
|---|---|
|
Indomethacin Therapy Patent Ductus Arteriosus |
Procedure: Withhold standard INDO dose if BNP < 100 pg/ml |
| Study Type: | Interventional |
| Study Design: | Diagnostic, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study |
| Enrollment: | 60 |
| Study Start Date: | April 2004 |
| Study Completion Date: | March 2007 |
Eligibility| Ages Eligible for Study: | up to 4 Months |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | HIC# 10946 |
| Study First Received: | July 10, 2007 |
| Last Updated: | July 10, 2007 |
| ClinicalTrials.gov Identifier: | NCT00500305 History of Changes |
| Health Authority: | United States: Institutional Review Board |
|
indomethacin therapy patent ductus arteriosus |
|
Natriuretic Peptide, Brain Heart Diseases Cardiovascular Abnormalities Natriuretic Agents Therapeutic Uses Physiological Effects of Drugs |
Cardiovascular Diseases Cardiovascular Agents Congenital Abnormalities Heart Defects, Congenital Pharmacologic Actions Ductus Arteriosus, Patent |