Indomethacin Suppositories |
Indocin Suppositories |
Clinical Trial: Indomethacin Germinal Matrix Hemorrhage/Intraventricular Hemorrage (GMH/IVH) Prevention Trial
This study is no longer recruiting patients.
|
Purpose
The purpose of this multicenter trial is to determine if indomethacin prevents bleeding in the brain of very low birth weight preterm infants.
| Condition | Treatment or Intervention | Phase |
|---|---|---|
| intraventricular hemorrhage (IVH) bleeding in the brain prematurity very low birth weight infants | Drug: indomethacin | Phase III |
MedlinePlus related topics: Stroke
Study Type: Interventional
Study Design: Prevention, Randomized, Placebo Control
Official Title: Randomized Indomethacin Germinal Matrix Hemorrhage/Intraventricular Hemorrage (GMH/IVH) Prevention Trial
Expected Total Enrollment: 505
Study start: September 1989
Intraventricular hemorrhage (IVH) or bleeding in the brain remains a major problem of preterm infants. This randomized, placebo-controlled multicenter trial enrolled 505 infants of 600 to 1250g birth weight to determine if indomethacin lowers the incidence of IVH. During this longitudinal trial, follow-up assessments have been performed at the ages of 3, 4 1/2, 6 and 8. The initial results at age 3 years revealed no advantages to the indomethacin group over and above the decreases in IVH, however, the results did show a significant increase in ventriculomegaly in the indomethacin negative or "placebo" group. Later results at 4 1/2 and 6 years of age showed beneficial effects of indomethacin on cognitive and behavioral outcomes over and above the effects on preventing IVH. The study investigators continue to followup with the children to find out if early use of indomethacin will continue to improve the outcomes of extremely low birth weight children.
Eligibility
Ages Eligible for Study: up to 6 Hours, Genders Eligible for Study: Both
Criteria
- Preterm infants < 1250 g birth weight
- Admitted to participating institution < 6 hrs of age
- No evidence for congenital malformations
- Cranial US at 6 postnatal hours without evidence of Grades III - IV intraventricular hemorrhage
Location Information
Connecticut
Yale University School of Medicine, New Haven, Connecticut, United States
Michigan
Maine Medical Center, Portland, Michigan, United States
Rhode Island
Brown University School of Medicine, Providence, Rhode Island, United States
Laura R. Ment, M.D., Principal Investigator, Department of Pediatrics, Yale University School of Medicine
More Information
Record last reviewed: October 2004
Last Updated: October 14, 2004
Record first received: April 12, 2002
ClinicalTrials.gov Identifier: NCT00033917
Health Authority: United States: Federal Government
ClinicalTrials.gov processed this record on 2005-04-08
Source: ClinicalTrials.gov
Cache Date: April 9, 2005
Resources
- Indocin Suppositories (Drug Digest)
- Indomethacin Suppositories (Drug Digest)

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