Vitamin A Supplementation for Extremely-Low-Birth-Weight Infants
Status: | Completed |
---|---|
Conditions: | Bronchitis, Obesity Weight Loss, Hospital, Women's Studies, Pulmonary, Pulmonary |
Therapuetic Areas: | Endocrinology, Pulmonary / Respiratory Diseases, Other, Reproductive |
Healthy: | No |
Age Range: | Any |
Updated: | 9/28/2017 |
Start Date: | January 1996 |
End Date: | July 1999 |
Randomized Trial of Vitamin A Supplementation for Extremely-Low-Birth-Weight
This multi-site, randomized trial was conducted to determine the safety and effectiveness of
a higher dose of vitamin A and determine if this would increase the rate of survival without
bronchopulmonary dysplasia (BPD) and reduce the risk of sepsis. Infants with birth weights
from 401-1000g and who were on mechanical ventilation or supplemental oxygen at 24-96 hours
of age were enrolled. Subjects were randomized to either the Vitamin A or a control group.
Infants in the Vitamin A group were given a dose of 5000 IU (0.1 ml) intramuscularly on
Mondays, Wednesdays, and Fridays for four weeks. Control infants received a sham procedure
rather than placebo injections.
a higher dose of vitamin A and determine if this would increase the rate of survival without
bronchopulmonary dysplasia (BPD) and reduce the risk of sepsis. Infants with birth weights
from 401-1000g and who were on mechanical ventilation or supplemental oxygen at 24-96 hours
of age were enrolled. Subjects were randomized to either the Vitamin A or a control group.
Infants in the Vitamin A group were given a dose of 5000 IU (0.1 ml) intramuscularly on
Mondays, Wednesdays, and Fridays for four weeks. Control infants received a sham procedure
rather than placebo injections.
Infants with extremely low birth weights (≤1,000 g) have low plasma and tissue concentrations
of vitamin A, and vitamin A deficiency may predispose these infants to chronic lung disease.
A meta-analysis of clinical trials of vitamin A supplementation for preterm infants revealed
a 17% increase in the rate of survival without chronic lung disease, which approached
statistical significance.
This multi-site, randomized trial was conducted to determine the safety and effectiveness of
a higher dose of vitamin A than that used in previous trials in extremely-low-birth-weight
(ELBW) infants. We hypothesized that vitamin A supplementation would increase the rate of
survival without bronchopulmonary dysplasia and reduce the risk of sepsis.
Infants with birth weights from 401-1000g and who received mechanical ventilation or
supplemental oxygen at 24-96 hours of age were enrolled. Subjects were randomized to either
the vitamin A or a control group. Infants in the Vitamin A group were given a dose of 5000 IU
(0.1 ml) intramuscularly on Mondays, Wednesdays, and Fridays for four weeks. Control infants
received a sham procedure rather than placebo injections.
Serum vitamin A was measured in a central laboratory at base line and at 28 days in the first
300 infants. On study day 28 (two to three days after the last treatment and immediately
after a blood sample was collected), the relative dose-response was evaluated.
of vitamin A, and vitamin A deficiency may predispose these infants to chronic lung disease.
A meta-analysis of clinical trials of vitamin A supplementation for preterm infants revealed
a 17% increase in the rate of survival without chronic lung disease, which approached
statistical significance.
This multi-site, randomized trial was conducted to determine the safety and effectiveness of
a higher dose of vitamin A than that used in previous trials in extremely-low-birth-weight
(ELBW) infants. We hypothesized that vitamin A supplementation would increase the rate of
survival without bronchopulmonary dysplasia and reduce the risk of sepsis.
Infants with birth weights from 401-1000g and who received mechanical ventilation or
supplemental oxygen at 24-96 hours of age were enrolled. Subjects were randomized to either
the vitamin A or a control group. Infants in the Vitamin A group were given a dose of 5000 IU
(0.1 ml) intramuscularly on Mondays, Wednesdays, and Fridays for four weeks. Control infants
received a sham procedure rather than placebo injections.
Serum vitamin A was measured in a central laboratory at base line and at 28 days in the first
300 infants. On study day 28 (two to three days after the last treatment and immediately
after a blood sample was collected), the relative dose-response was evaluated.
Inclusion Criteria:
- Infants wtih birth weights from 401-1,000g
- Receiving mechanical ventilation or supplemental oxygen at 24-96 hours of age
Exclusion Criteria:
- Major congenital anomalies
- Congenital nonbacterial infection
- Infants diagnosed with a terminal illness (as indicated by a pH below 6.80 or by the
presence of hypoxia with bradycardia for more than two hours)
- Infants who were to receive vitamin A in a parenteral fat emulsion or in doses
exceeding recommendations for multivitamin preparations
We found this trial at
11
sites
Emory University Emory University, recognized internationally for its outstanding liberal artscolleges, graduate and professional schools,...
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Univ of Texas, Southwestern Med Ctr of Dallas The story of UT Southwestern Medical Center...
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Indiana University INDIANA UNIVERSITY is a major multi-campus public research institution, grounded in the liberal...
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University of Miami A private research university with more than 15,000 students from around the...
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Yale University Yale's roots can be traced back to the 1640s, when colonial clergymen led...
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