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The 1000 First Day of Life : Effect of Multi Micronutrients Supplementation on Pregnancy Outcomes

The 1000 First Day of Life : Effect of Multi Micronutrients Supplementation on Pregnancy Outcomes

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06035315
Enrollment
240
Registered
2023-09-13
Start date
2023-05-01
Completion date
2024-08-31
Last updated
2023-09-13

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

Conditions

Maternal Care Patterns, Maternal-Fetal Relations, Maternal Outcome, Nutritional Deficiency, Nutrition, Healthy, Perinatal Outcome

Brief summary

To monitor the effects of multi micronutrients supplementations during pregnancy towards pregnancy outcomes

Detailed description

A randomized control trial of two clusters : 1st cluster without giving multi micronutrients; 2nd cluster giving multi micronutrients. Differences between cluster : Additional multi micronutrients by giving : Complete multi micronutrients, calcium, vitamin D and DHA. The additional multi micronutrients were given since 1st until 3rd trimester for interventions group. There are also additional laboratory examinations for intervention group : Vitamin D, Lipid Profile and Zinc level. In control group : we use standard public health care micronutrients (Iron supplementation and calcium); and standard blood examinations. Ultrasound examination was performed for both cluster since 1st until 3rd trimester.

Interventions

DIETARY_SUPPLEMENTMultiple Micronutrients during pregnancy

Pregnant women examine since 8 weeks gestation are being followed until delivery; are given additional micronutrients (Complete multi micronutrients-Calcium-Vitamin D-DHA); and perform ultrasound examinations each trimester and additional laboratory examination (Vitamin D level-Lipid profile-Zinc)

Sponsors

Dr Cipto Mangunkusumo General Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Intervention model description

Randomized control trial : comparison of two clusters

Eligibility

Sex/Gender
FEMALE
Age
15 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* First trimester pregnancy * Gestational age \< 10 weeks gestation * Agree as research participant * Living in DKI Jakarta

Exclusion criteria

* Assisted Reproductive * History of PCOS * History of Chronic Hypertension * History of Diabetes Mellitus * History of Preeclampsia * Maternal chronic disease : Cardiovascular disease; Autoimmune condition; Malignancy) * Plan to move from Jakarta prior or during pregnancy * History of Recurrent pregnancy loss

Design outcomes

Primary

MeasureTime frameDescription
Maternal Outcome1 yearMaternal Death; Preterm Delivery; Preeclampsia; Intrauterine Infections; Post partum hemorrhage
Perinatal Outcome1 yearNeonatal death; Low birth weight; Intra uterine growth restriction; Asphyxia

Countries

Indonesia

Contacts

Primary ContactYurika Elizabeth, Medical Doctor
yurika.elizabeth.s@gmail.com+62 8999979916
Backup ContactAmanda Rumondang, Obstetrician Gynecologist
amanda17.md@gmail.com+62 81318375211

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026