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Evaluation of the Impact of the WHO Recommended Vitamin A Supplementation at First Immunisation Contact After 6 Months of Age
This study is currently recruiting participants.
Verified by Bandim Health Project, November 2008
First Received: August 8, 2007   Last Updated: November 6, 2008   History of Changes
Sponsor: Bandim Health Project
Collaborators: Ministry of Health, Guinea-Bissau
University of Aarhus
Information provided by: Bandim Health Project
ClinicalTrials.gov Identifier: NCT00514891
  Purpose

High-dose vitamin A to children above 6 months of age reduces all-cause mortality by 23-30%. The WHO recommends vitamin A supplementation (VAS) with the first vaccine after 6 months of age. However, the effect of providing VAS with vaccines has never been investigated. We have hypothesised that the effect of VAS depends on the immune stimulus at the time of supplementation. Hence, the effect might vary depending on which type of vaccine it is given with. In particular, we hypothesised that VAS might be beneficial when given with measles vaccine but not when given with DTP vaccine. Normally the first vaccine after 6 months of age would be a measles vaccine, but many children come late for their DTP vaccinations and receive DTP alone or together with measles vaccine. Hence, it is important to study whether the effect of VAS is the same irrespective of the vaccine(s) administered at the same time.

Guinea-Bissau has not yet implemented the WHO vitamin A policy of providing VAS with vaccines, but plans to do so within the next years. Together with the Ministry of Health in Guinea-Bissau, the Bandim Health Project (BHP) in Guinea-Bissau will investigate the effect on mortality and morbidity of implementing the WHO vitamin A policy in Guinea-Bissau. This will be done in a large randomised trial.

BHP has a demographic surveillance system (DSS) which has followed a population of now more than 150,000 individuals for almost 30 years. Children will be randomised to receive VAS or placebo with their first vaccine after 6 months of age, and will be followed through the DSS to assess mortality and morbidity. Based on previous observations, the effects of VAS might differ according to sex and season. The interaction between VAS, sex, and season will also be studied in the present trial. By identifying situations where VAS may be beneficial, ineffective, or even harmful the study may contribute importantly to optimising the VAS policy for low-income countries.


Condition Intervention Phase
Mortality
Morbidity
Biological: Vitamin A
Phase IV

Study Type: Interventional
Study Design: Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment
Official Title: Evaluation of the Impact on Mortality and Morbidity of the WHO Recommended Vitamin A Supplementation at First Immunisation Contact After 6 Months of Age

Resource links provided by NLM:


Further study details as provided by Bandim Health Project:

Primary Outcome Measures:
  • Mortality, morbidity

Secondary Outcome Measures:
  • Growth, Vitamin A status, Immunology

Study Start Date: August 2007
Arms Assigned Interventions
1: Active Comparator
Vitamin A supplementation
Biological: Vitamin A
The effect of vitamin A given with different vaccines will be studied
2: Placebo Comparator
Placebo
Biological: Vitamin A
The effect of vitamin A given with different vaccines will be studied

  Eligibility

Ages Eligible for Study:   6 Months to 23 Months
Genders Eligible for Study:   Both
Criteria

Inclusion Criteria:

  • Urban area: 6-17-month-old children, presenting for vaccination at a health centre in the study area.
  • Rural area: 6-23-month-old children who are missing one or more routine vaccinations when visited by our mobile team.

Exclusion Criteria:

  • Normally applied contraindications for receiving vaccinations, including high fever.
  • VAS within last month.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00514891

Contacts
Contact: Ane B Fisker, MD +245 201489 a.fisker@bandim.org
Contact: Christina Rasmussen, MSc +45 32683162 crn@ssi.dk

Locations
Guinea-Bissau
Bandim Health Project, Apartado 861 Recruiting
Bissau, Guinea-Bissau
Contact: Peter Aaby     +245 01489     p.aaby@bandim.org    
Sub-Investigator: Peter Aaby            
Sponsors and Collaborators
Bandim Health Project
Ministry of Health, Guinea-Bissau
University of Aarhus
Investigators
Principal Investigator: Christine S Benn, MD, PhD Bandim Health Project, Statens Serum Institut, Artillerivej 5, 2300 Copenhagen S, Denmark
Study Director: Peter Aaby, Dr.Med. Bandim Health Project, Apartado 861, 1004 Bissau Codex, Guinea-Bissau
  More Information

No publications provided

Study ID Numbers: CVK-2006-7041-99
Study First Received: August 8, 2007
Last Updated: November 6, 2008
ClinicalTrials.gov Identifier: NCT00514891     History of Changes
Health Authority: Guinea-Bissau: Ministry of Health;   Denmark: Ethics Committee

Additional relevant MeSH terms:
Anticarcinogenic Agents
Antioxidants
Molecular Mechanisms of Pharmacological Action
Antineoplastic Agents
Growth Substances
Physiological Effects of Drugs
Protective Agents
Pharmacologic Actions
Retinol palmitate
Vitamin A
Vitamins
Therapeutic Uses
Micronutrients

ClinicalTrials.gov processed this record on November 09, 2009