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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03308487
Other study ID # IR.SBMU.RETECH.1395.631
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2017
Est. completion date September 2018

Study information

Verified date February 2019
Source National Nutrition and Food Technology Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Groups (group 1 receives 1000 IU vitamin D and group 2 receives 2000 IU vitamin D) through a random allocation. It is necessary to mention that all cases in each group could be able to receive the current supplementation during pregnancy (Folic acid, iron and multivitamin and calcium). This study aimed to evaluate the efficacy of two doses of vitamin D supplementation (1000 and 2000 IU/d) during pregnancy on maternal and newborn vitamin D status and metabolic profile including lipid profile (serum concentration of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglyceride(TG)), glucose homeostasis (fasting glucose, insulin, insulin resistance (HOMA-IR)) and inflammatory and oxidative stress (OS) markers and pregnancy outcomes including gestational diabetes, preeclampsia, preterm delivery, abortion, cesarian section, and also anthropometric data and apgar score of infants compared with placebo.


Description:

In this randomized controlled trial, 84 pregnant women aged at 18-40 years with gestational age of <12 weeks will be recruited and divided into 2 groups.

Demographic, socioeconomic and lifestyle data as well as blood samples and urine samples will be collected at baseline and in the last month of pregnancy. Moreover the cord blood will be collected at birth.

Fasting blood glucose, insulin resistance (HOMA-IR), insulin, lipid profile (serum concentration of total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglyceride(TG)), inflammatory (IL-1β, IL-6, TNF-α, hs-CRP) and oxidative stress markers (MDA, TAC), calcium:creatinine ratio are going to be evaluated at the beginning and in the end of the interventional period in pregnant women. Inflammatory (IL-1β, IL-6, Tumor Necrosis Factor (TNF-α), hs-CRP) and oxidative stress markers (MDA, TAC) will be determined in cord blood as well.


Recruitment information / eligibility

Status Completed
Enrollment 84
Est. completion date September 2018
Est. primary completion date January 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- maternal age of 18-40 years,

- gestational age of 12 weeks or less,

- singleton pregnancies,

- mothers supposed to have normal pregnancy and not having preexisting diseases like hypertension, or cardiac, renal, hepatic, autoimmune , rheumatoid arthritis and digestive disease, or endocrinological disorders including diabetes (type 1 or type 2 diabetes), parathyroid disorders, and thyroid disorder,

- not receiving dietary supplements including vitamin D (>600 IU/d), or omega-3 within the past 3 months before the intervention,

- not taking medications that could potentially influence vitamin D metabolism,

- willingness to participate in the study.

Exclusion Criteria:

- Participants who do not meet the inclusion criteria,

- those who diagnosed to have fasting blood sugar (FBS)>92 at first blood sampling and/or blood pressure > 140/90 mmHg at the first visit,

- using extra vitamin D3 supplement and/or omega-3 and/or other medications that could potentially influence vitamin D metabolism,

- fetal anomaly,

- poor adherence to the study protocol,

- unwillingness to continue the intervention.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
vitamin D3 (1000 IU)

Vitamin D3 (2000 IU)


Locations

Country Name City State
Iran, Islamic Republic of National Nutrition and Food Technology Research Institute Tehran

Sponsors (2)

Lead Sponsor Collaborator
Tirang R. Neyestani, Ph.D. National Nutrition and Food Technology Institute

Country where clinical trial is conducted

Iran, Islamic Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary The changes in maternal vitamin D status from first trimester to last month of pregnancy The serum concentration of 25(OH) D will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of fasting blood glucose from first trimester to last month of pregnancy The serum concentration of fasting blood glucose will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of insulin from first trimester to last month of pregnancy The serum concentration of insulin will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of total cholesterol (TC) from first trimester to last month of pregnancy The serum concentration of total cholesterol (TC) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of low-density lipoprotein cholesterol (LDL-C) from first trimester to last month of pregnancy The serum concentration of low-density lipoprotein cholesterol (LDL-C) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of high-density lipoprotein cholesterol (HDL-C) from first trimester to last month of pregnancy The serum concentration of high-density lipoprotein cholesterol (HDL-C) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of triglyceride(TG) from first trimester to last month of pregnancy The serum concentration of triglyceride(TG) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in systolic blood pressure from first trimester to last month of pregnancy systolic and diastolic blood pressure will be measured by a training physician baseline and 6-8 months
Secondary The changes in diastolic blood pressure from first trimester to last month of pregnancy systolic and diastolic blood pressure will be measured by a training physician baseline and 6-8 months
Secondary preeclampsia Preeclampsia characterized by high blood pressure begins after 20 weeks of pregnancy in women whose blood pressure had been normal. 2-5 months
Secondary Preterm delivery A premature birth is a birth that takes place before the start of the 37th week of pregnancy. 5-8 months
Secondary Spontaneous abortion Spontaneous abortion is the natural death of an embryo or fetus before 20 weeks of gestation. 2-5 months
Secondary The changes in cellular secretion of interleukin 1 from first trimester to last month of pregnancy The status of interleukin 1 will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in cellular secretion of interleukin 6 from first trimester to last month of pregnancy The status of interleukin 6 will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in cellular secretion of interleukin 10 from first trimester to last month of pregnancy The status of interleukin 10 will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in cellular secretion of TNF-a from first trimester to last month of pregnancy The status of TNF-a will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of hs-CRP from first trimester to last month of pregnancy The status of hs-CRP will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of MDA (Malondialdehyde) from first trimester to last month of pregnancy the serum concentration of MDA (Malondialdehyde) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of TAC from first trimester to last month of pregnancy the serum concentration of TAC will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of parathyroid hormone (PTH) from first trimester to last month of pregnancy the serum concentration of parathyroid hormone (PTH) will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of calcium from first trimester to last month of pregnancy the serum concentration of calcium will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary The changes in serum concentration of phosphate from first trimester to last month of pregnancy the serum concentration of phosphate will be measured during the first trimester and last month of pregnancy. baseline and 6-8 months
Secondary Apgar score The Apgar score is a quick evaluation of one minute and five minutes after birth which tests the birthing process and readiness of newborn to meet the world without additional medical assistance. 6-8 months
Secondary The weight measures of newborn The data of anthropometric measures including weight will be measured. 6-8 months
Secondary The height measures of newborn The data of anthropometric measures including height will be measured. 6-8 months
Secondary The head circumference measures of newborn The data of anthropometric measures including head circumference will be measured. 6-8 months
See also
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