Full Text View
Tabular View
No Study Results Posted
Related Studies
Trial of Indomethacin Prophylaxis in Preterm Infants (TIPP)
This study has been completed.
First Received: February 1, 2001   Last Updated: January 26, 2007   History of Changes
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)

Resource links provided by NLM:


Further study details as provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):

Estimated Enrollment: 1202
Study Start Date: November 1993
Estimated Study Completion Date: April 2000
Detailed Description:

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
Criteria

Inclusion Criteria:

  • Birth weight 500 to 999 grams;
  • Postnatal age greater than 2 hours;

Exclusion Criteria:

  • Unable to administer study drug within 6 hours of birth;
  • Structural heart disease and/or renal disease;
  • Dysmorphic features or congenital abnormalities;
  • Tocolytic therapy with indomethacin or other prostaglandin inhibitor within 72 hours prior to delivery;
  • Overt clinical bleeding from more than one site;
  • Platelet count less than 50 x 109/L;
  • Hydrops;
  • Not considered viable
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00009646

Sponsors and Collaborators
Medical Research Council of Canada
Investigators
Principal Investigator: Barbara Schmidt, MD McMaster University
  More Information

Additional Information:
Publications:
Additional publications automatically indexed to this study by National Clinical Trials Identifier (NCT ID):
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

Keywords provided by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD):
Chronic lung disease
Indocin
Indomethacin
Infants, very low birth weight
Intraventricular hemorrhage
Necrotizing enterocolitis
Patent ductus arteriosus
Pulmonary hemorrhage

Additional relevant MeSH terms:
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

ClinicalTrials.gov processed this record on November 27, 2009