Skip to content

Improving the nutrition of pregnant women through a multiple micronutrient fortified salt

A study to improve the vitamin A and iodine status of pregnant women through a multiple micronutrient fortified salt

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17782574
Enrollment
300
Registered
2022-02-19
Start date
2007-05-12
Completion date
Unknown
Last updated
2022-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Vitamin A levels in the three trimesters and urinary iodine levels in the first and last trimester of pregnancy in pregnant women Nutritional, Metabolic, Endocrine

Interventions

The women who visited the antenatal clinic were recruited into the study and would fall into the experimental or control group based on which week they visited the antenatal clinic. The women would be

Sponsors

Sundar Serendipity Foundation
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Pregnant women 2. Aged 19 to 29 years 3. In the first trimester of pregnancy 4. Written informed consent

Exclusion criteria

Exclusion criteria: 1. Pregnant women with hemoglobin less than 8 g/dl were excluded so that they could be treated immediately for anaemia 2. Women with current or previous gynecological problems

Design outcomes

Primary

MeasureTime frame
1. Serum vitamin A in the first, second and third trimester of pregnancy, measured by a rapid reverse-phase high-performance liquid chromatography (HPLC-Shimadzu, Japan) at baseline, midpoint after 3 months and endline after 6 months 2. Urinary iodine in the first trimester and third trimester of pregnancy, measured by spectrophotometry at baseline and endline after 6 months

Secondary

MeasureTime frame
1. The age and parity of the pregnant women collected using a questionnaire during enrollment into the study 2. Night blindness assessed using a questionnaire during enrollment into the study, and at the second- (midpoint after 3 months) and third-trimester visits (endline after 6 months) of the pregnant women to the hospital 3. The number of days the fortified salt was not used in the past 3 months in the experimental group, assessed by asking the women when they came to the clinic in their second (midpoint after 3 months) and third trimester (endline after 6 months)

Countries

India

Contacts

Public ContactMalavika Vinod Kumar
malavika@sundarserendipityfoundation.org+91 (0)9840323091

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 11, 2026