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| Sponsor: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
|---|---|
| Collaborator: |
Medical Research Council of Canada |
| Information provided by: | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
| ClinicalTrials.gov Identifier: | NCT00009646 |
Purpose
This trial will determine whether giving low-dose indomethacin to infants weight 500 to 999 grams (approximately 1 to 2 pounds) at birth improves their survival without cerebral palsy or developmental problems at 18 to 22 months of age.
| Condition | Intervention | Phase |
|---|---|---|
|
Infant, Very Low Birth Weight Infant, Premature Ductus Arteriosus, Patent |
Drug: indomethacin |
Phase III |
| Study Type: | Interventional |
| Study Design: | Prevention, Randomized, Double-Blind, Placebo Control, Single Group Assignment, Efficacy Study |
| Official Title: | Trial of Indomethacin Prophylaxis in Preterm Infants (TIPP) |
| Estimated Enrollment: | 1202 |
| Study Start Date: | November 1993 |
| Estimated Study Completion Date: | April 2000 |
Prophylactic indomethacin reduces patent ductus arteriosus (PDA) and intraventricular hemorrhage in very low birth weight infants. However, the effects of early indomethacin on long-term neurodevelopment remain uncertain. There is also insufficient evidence to rule out serious adverse effects, such as increases in the risk of necrotizing enterocolitis (NEC) and retinopathy of prematurity (ROP). The aim of this trial was to determine if prophylactic administration of indomethacin improves survival without neurosensory impairments in extremely-low-birth-weight infants. Infants (n=1202) with birthweights 500 to 999 grams were randomized between 2 and 6 hours after birth to receive either intravenous indomethacin (0.1 mg/kg) or equal volumes of normal saline placebo, daily for 3 days. The primary outcomes at a corrected age of 18 months was a composite of death, cerebral palsy, cognitive delay, deafness, or blindness. Secondary long-term outcomes were hydrocephalus necessitating the placement of a shunt, seizure disorder, and microcephaly. Secondary short-term outcomes were patent ductus arteriosus, pulmonary hemorrhage, chronic lung disease, cranial ultrasonographic abnormalities, nectrotizing enterocolitis and retinopathy. Infants were evaluated in follow-up at 18-22 months corrected age.
Eligibility| Ages Eligible for Study: | up to 6 Hours |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations
More Information
| Study ID Numbers: | NICHD-1007, U10 HD34216, U10 HD27904, U10 HD21364, U10 HD27851, U10 HD21397, U10 HD27881, U10 HD27880, U10 HD21373, U10 HD21385 |
| Study First Received: | February 1, 2001 |
| Last Updated: | January 26, 2007 |
| ClinicalTrials.gov Identifier: | NCT00009646 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Chronic lung disease Indocin Indomethacin Infants, very low birth weight |
Intraventricular hemorrhage Necrotizing enterocolitis Patent ductus arteriosus Pulmonary hemorrhage |
|
Anti-Inflammatory Agents Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Reproductive Control Agents Gout Suppressants Body Weight Signs and Symptoms Tocolytic Agents Sensory System Agents Therapeutic Uses Indomethacin Cardiovascular Diseases Anti-Inflammatory Agents, Non-Steroidal Analgesics |
Congenital Abnormalities Ductus Arteriosus, Patent Birth Weight Heart Diseases Cardiovascular Abnormalities Cyclooxygenase Inhibitors Enzyme Inhibitors Cardiovascular Agents Pharmacologic Actions Analgesics, Non-Narcotic Peripheral Nervous System Agents Antirheumatic Agents Central Nervous System Agents Heart Defects, Congenital |