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Impact of Maternal Supplementation With Dual Megadose of Vitamin A

I

Instituto Materno Infantil Prof. Fernando Figueira

Status and phase

Completed
Phase 3
Phase 2

Conditions

Vitamin A Deficiency
Hypovitaminosis

Treatments

Dietary Supplement: vitamin A
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT00742937
IMIPVITA-001

Details and patient eligibility

About

The purpose of this study is to evaluate the effect of maternal supplementation with 400,000 IU of oral retinol palmitate in the post-partum, the nutritional situation of the binomial mother-child, on growth and morbidity of children in breastfeeding in the first six months of life.

Full description

The effect will be assessed by the milk and blood.

Enrollment

239 patients

Sex

Female

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Pregnant low-risk obstetric

Exclusion criteria

  • Premature birth
  • Newborn babies with birth defects and / or other serious diseases

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

239 participants in 2 patient groups, including a placebo group

A
Placebo Comparator group
Description:
After birth the women will receive one capsule 200,000 UI of retinol palmitate (vitamin A)plus vitamin E and eight days after delivery the second capsule of vitamin E will be administer.
Treatment:
Dietary Supplement: Placebo
B
Experimental group
Description:
After birth the women will receive one capsule 200,000 UI of retinol palmitate (vitamin A)plus vitamin E and eight days after delivery the second capsule of 200,000 UI of retinol palmitate (vitamin A)plus vitamin E will be administer.
Treatment:
Dietary Supplement: vitamin A

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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