search
Back to results

Trial of Vitamin D Supplements to Raise Calcidiol Levels of Pregnant Women in Mongolia

Primary Purpose

Pregnancy, Vitamin D Deficiency

Status
Completed
Phase
Not Applicable
Locations
Mongolia
Study Type
Interventional
Intervention
600 IU Vitamin D3 in prenatal vitamin
2000 IU Vitamin D3 in prenatal vitamin
4000 IU Vitamin D3 in prenatal vitamin
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Pregnancy focused on measuring pregnancy, Mongolia, Vitamin D, preeclampsia

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Age 18 or older
  • 12-16 weeks pregnant
  • Receiving prenatal care at Zuun Kharaa Hospital and planning to deliver at Zuun Kharaa Hospital
  • Willing not to take any additional vitamin D supplements, other than the study dispensed pills

Exclusion Criteria:

  • Existing known seizure disorder, renal failure, parathyroid disease, thyroid disease, sarcoidosis, cancer, or tuberculosis. (Tuberculosis is routinely screened in pregnancy)
  • History of kidney stones
  • Known sensitivity to multivitamin preparations
  • Taking vitamin D supplements containing >600 IU/day.

Sites / Locations

  • Zuun Kharaa Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

600 IU

2000 IU

4000 IU

Arm Description

Women will receive prenatal vitamins containing 600 IU of Vitamin D.

Women will receive prenatal vitamins containing 2000 IU of Vitamin D.

Women will receive prenatal vitamins containing 4000 IU of Vitamin D.

Outcomes

Primary Outcome Measures

Total Serum 25(OH)D Concentration
Circulating vitamin D at the end of the study as measured by VIDAS® enzyme linked fluorescent assay (ELFA)

Secondary Outcome Measures

The Number of Participants With Preeclampsia
Preeclampsia as measured by new onset hypertension after 20 weeks gestation and proteinuria.
Average Monthly Blood Pressure
Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) were measured in mm Hg at each antenatal care visit by the Study Coordinator, using the Omron- Elite 7300 (Omron Healthcare, Bannockburn, Illinois, USA) automated blood pressure monitor. Three blood pressure readings were taken after at least five minutes seated rest. For the analysis of mean blood pressures at each antenatal visit, the three readings were averaged for each participant.
Arterial Tonometry
Investigators will assess Augmentation Index (AIx) and Pulse Wave Velocity (PWV) by study arm, as measured by AtCor Medical SphygmoCor device. THIS TONOMETER FAILED AND COULD NOT BE REPAIRED, SO WE ARE NOT PRESENTING THESE DATA AS OUTCOMES.
Number of Patients With Preterm Delivery as Measured by Clinical Diagnosis
Gestational age was determined clinically by last menstrual period and by routine first trimester ultrasound which was universal; where these differed by more than 10 days, the ultrasound date was used. Gestational age at delivery was recorded by clinicians and rounded to the nearest week. Preterm delivery was defined as delivery before the 37th week of gestation.
Casarean Section as Measured by Medical Record Abstraction
Cesarean section was abstracted from the labor and delivery chart.
Assisted Vaginal Delivery as Measured by Medical Record Abstraction
Assisted vaginal delivery with forceps delivery was abstracted from the labor and delivery chart.
Number of Small for Gestational Age (SGA) Neonates as Measured by Medical Record Abstraction
SGA defined by the lowest 10th percentiles of sex-specific birthweight for gestational age charts of the INTERGROWTH-21st study
Number of Large for Gestational Age (LGA) Neonates as Measured by Medical Record Abstraction
LGA defined by the highest 10th percentiles of sex-specific birthweight for gestational age charts of the INTERGROWTH-21st study
Mean Calcemia as Measured by Serum Calcium Test (2mo)
Measured on a semi-automated photometer (Humalyzer 3500, Human Diagnostics, Magdeburg, Germany)
Number of Patients With Proteinuria as Measured by Urine Dipstick
Proteinuria at last antenatal visit (usually 36-40 weeks' gestation), measured by 1+ Standard Diagnostics UroColor 10 10 (Kyonggi-do, South Korea) reagent strips
Number of Patients With Hypertensive Disorders of Pregnancy as Measured by Clinical Diagnosis
In Mongolia, clinician-diagnosed preeclampsia may include a blood pressure increases >30 mm Hg above early pregnancy, with or without documented hypertension, proteinuria, or symptoms such as headache and edema
Number of Patients With Bacterial Vaginosis as Measured by Potassium Hydroxide (KOH) Wet Mount
Bacterial vaginosis was routinely screened by potassium hydroxide wet mount at the first antenatal visit, at 28 weeks' and 32 weeks' gestation. It was also diagnosed by whiff test. We included both wet mount and whiff test positive in the bacterial vaginosis endpoint
Mean Calcemia as Measured by Serum Calcium Test (36-40 Weeks)
Measured on a semi-automated photometer (Humalyzer 3500, Human Diagnostics, Magdeburg, Germany)

Full Information

First Posted
February 11, 2015
Last Updated
February 26, 2021
Sponsor
Brigham and Women's Hospital
Collaborators
National Center for Maternal and Child Health Research, Mongolia, Zuun Kharaa Hospital
search

1. Study Identification

Unique Protocol Identification Number
NCT02395081
Brief Title
Trial of Vitamin D Supplements to Raise Calcidiol Levels of Pregnant Women in Mongolia
Official Title
Trial of Vitamin D Supplements to Raise Calcidiol Levels of Pregnant Women in Mongolia
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
February 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
December 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
National Center for Maternal and Child Health Research, Mongolia, Zuun Kharaa Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A double-blind randomized, placebo-controlled trial comparing the impact of 600 IU, 2000 IU, or 4000 IU of Vitamin D3 on third trimester 25(OH)D levels and change from baseline. The Vitamin D will be integrated in a standard prenatal vitamin, which will be taken from 12-16 weeks' gestation and continue throughout pregnancy. Umbilical cord 25(OH)D levels will also be determined. The investigators will generate preliminary data regarding Vitamin D intake and hypertensive disorders, blood pressure, and arterial function measured by tonography. The investigators will independently test blood pressure and proteinuria to identify preeclampsia cases.
Detailed Description
Vitamin D deficiency (serum 25(OH)D levels <20 ng/ml or 50 nmol/l) is widespread among Mongolians and is nearly universal during the winter months. The investigators have conducted a series of studies which have shown nearly universal Vitamin D deficiency in the winter months. Observational studies in the U.S. have linked low 25(OH)D levels in women to a higher risk of preeclampsia. Mongolians also report levels of preeclampsia that are 3 times higher than those in the U.S (official reports cite 15%, though this may include gestational hypertension). Given the widespread Vitamin D deficiency in Mongolian women, the high prevalence of hypertensive pregnancy in Mongolia, and the observational studies linking low 25(OH)D levels with preeclampsia risk, the investigators are conducting a pilot Vitamin D dosing trial to: Determine what level of Vitamin D supplementation is needed to secure 25(OH)D levels of at least 20 ng/ml in pregnant Mongolian women Generate preliminary data in support of a funding application for a larger trial of Vitamin D supplements to prevent preeclampsia in Mongolia A double-blind randomized, placebo-controlled trial comparing the impact of 600 IU, 2000 IU, or 4000 IU of Vitamin D3 on third trimester 25(OH)D levels and change from baseline. The Vitamin D will be integrated in a standard prenatal vitamin, which will be taken from 12-16 weeks' gestation and continue throughout pregnancy. Umbilical cord 25(OH)D levels will also be determined. The investigators will generate preliminary data regarding Vitamin D intake and hypertensive disorders, blood pressure, and arterial function measured by tonography. The investigators will independently test blood pressure and proteinuria to identify preeclampsia cases. The investigators will enroll 360 women who plan to receive their prenatal care and deliver at Zuun Kharaa Hospital in the Selenge province in northern Mongolia. Enrollment will be stratified by season. 120 women will be randomized to each of the three doses of vitamin D (600, 2000, 4000 IU) included in a standard prenatal vitamin. Calcemia will be monitored two months after randomization and weeks 36-40 of pregnancy. Adverse events of pregnancy will be reported to the Data Safety and Monitoring Board (DSMB) and Institutional Review Board (IRB) per protocol. Data will be gathered by a Mongolian study coordinator and local clinicians. A DSMB comprised of a U.S. and Mongolian clinicians and statisticians will monitor study data for safety.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Vitamin D Deficiency
Keywords
pregnancy, Mongolia, Vitamin D, preeclampsia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
360 (Actual)

8. Arms, Groups, and Interventions

Arm Title
600 IU
Arm Type
Placebo Comparator
Arm Description
Women will receive prenatal vitamins containing 600 IU of Vitamin D.
Arm Title
2000 IU
Arm Type
Experimental
Arm Description
Women will receive prenatal vitamins containing 2000 IU of Vitamin D.
Arm Title
4000 IU
Arm Type
Experimental
Arm Description
Women will receive prenatal vitamins containing 4000 IU of Vitamin D.
Intervention Type
Dietary Supplement
Intervention Name(s)
600 IU Vitamin D3 in prenatal vitamin
Intervention Description
Women will receive 600 IU 25(OH)D in prenatal vitamin.
Intervention Type
Dietary Supplement
Intervention Name(s)
2000 IU Vitamin D3 in prenatal vitamin
Intervention Description
Women will receive 2000 IU 25(OH)D in prenatal vitamin.
Intervention Type
Dietary Supplement
Intervention Name(s)
4000 IU Vitamin D3 in prenatal vitamin
Intervention Description
Women will receive 4000 IU 25(OH)D in prenatal vitamin.
Primary Outcome Measure Information:
Title
Total Serum 25(OH)D Concentration
Description
Circulating vitamin D at the end of the study as measured by VIDAS® enzyme linked fluorescent assay (ELFA)
Time Frame
36 weeks gestation or delivery, if delivery occurred before 36 weeks
Secondary Outcome Measure Information:
Title
The Number of Participants With Preeclampsia
Description
Preeclampsia as measured by new onset hypertension after 20 weeks gestation and proteinuria.
Time Frame
After 20 weeks gestation
Title
Average Monthly Blood Pressure
Description
Systolic Blood Pressure (SBP) and Diastolic Blood Pressure (DBP) were measured in mm Hg at each antenatal care visit by the Study Coordinator, using the Omron- Elite 7300 (Omron Healthcare, Bannockburn, Illinois, USA) automated blood pressure monitor. Three blood pressure readings were taken after at least five minutes seated rest. For the analysis of mean blood pressures at each antenatal visit, the three readings were averaged for each participant.
Time Frame
During pregnancy
Title
Arterial Tonometry
Description
Investigators will assess Augmentation Index (AIx) and Pulse Wave Velocity (PWV) by study arm, as measured by AtCor Medical SphygmoCor device. THIS TONOMETER FAILED AND COULD NOT BE REPAIRED, SO WE ARE NOT PRESENTING THESE DATA AS OUTCOMES.
Time Frame
36 weeks gestation
Title
Number of Patients With Preterm Delivery as Measured by Clinical Diagnosis
Description
Gestational age was determined clinically by last menstrual period and by routine first trimester ultrasound which was universal; where these differed by more than 10 days, the ultrasound date was used. Gestational age at delivery was recorded by clinicians and rounded to the nearest week. Preterm delivery was defined as delivery before the 37th week of gestation.
Time Frame
During pregnancy
Title
Casarean Section as Measured by Medical Record Abstraction
Description
Cesarean section was abstracted from the labor and delivery chart.
Time Frame
Delivery
Title
Assisted Vaginal Delivery as Measured by Medical Record Abstraction
Description
Assisted vaginal delivery with forceps delivery was abstracted from the labor and delivery chart.
Time Frame
Delivery
Title
Number of Small for Gestational Age (SGA) Neonates as Measured by Medical Record Abstraction
Description
SGA defined by the lowest 10th percentiles of sex-specific birthweight for gestational age charts of the INTERGROWTH-21st study
Time Frame
Delivery
Title
Number of Large for Gestational Age (LGA) Neonates as Measured by Medical Record Abstraction
Description
LGA defined by the highest 10th percentiles of sex-specific birthweight for gestational age charts of the INTERGROWTH-21st study
Time Frame
Delivery
Title
Mean Calcemia as Measured by Serum Calcium Test (2mo)
Description
Measured on a semi-automated photometer (Humalyzer 3500, Human Diagnostics, Magdeburg, Germany)
Time Frame
2 months after randomization
Title
Number of Patients With Proteinuria as Measured by Urine Dipstick
Description
Proteinuria at last antenatal visit (usually 36-40 weeks' gestation), measured by 1+ Standard Diagnostics UroColor 10 10 (Kyonggi-do, South Korea) reagent strips
Time Frame
36-40 weeks gestation/delivery
Title
Number of Patients With Hypertensive Disorders of Pregnancy as Measured by Clinical Diagnosis
Description
In Mongolia, clinician-diagnosed preeclampsia may include a blood pressure increases >30 mm Hg above early pregnancy, with or without documented hypertension, proteinuria, or symptoms such as headache and edema
Time Frame
During pregnancy
Title
Number of Patients With Bacterial Vaginosis as Measured by Potassium Hydroxide (KOH) Wet Mount
Description
Bacterial vaginosis was routinely screened by potassium hydroxide wet mount at the first antenatal visit, at 28 weeks' and 32 weeks' gestation. It was also diagnosed by whiff test. We included both wet mount and whiff test positive in the bacterial vaginosis endpoint
Time Frame
During pregnancy
Title
Mean Calcemia as Measured by Serum Calcium Test (36-40 Weeks)
Description
Measured on a semi-automated photometer (Humalyzer 3500, Human Diagnostics, Magdeburg, Germany)
Time Frame
36-40 weeks of pregnancy/delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age 18 or older 12-16 weeks pregnant Receiving prenatal care at Zuun Kharaa Hospital and planning to deliver at Zuun Kharaa Hospital Willing not to take any additional vitamin D supplements, other than the study dispensed pills Exclusion Criteria: Existing known seizure disorder, renal failure, parathyroid disease, thyroid disease, sarcoidosis, cancer, or tuberculosis. (Tuberculosis is routinely screened in pregnancy) History of kidney stones Known sensitivity to multivitamin preparations Taking vitamin D supplements containing >600 IU/day.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Janet Rich-Edwards, ScD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zuun Kharaa Hospital
City
Selenge
State/Province
Selenge Aimag
Country
Mongolia

12. IPD Sharing Statement

Citations:
PubMed Identifier
30552064
Citation
Enkhmaa D, Tanz L, Ganmaa D, Enkhtur S, Oyun-Erdene B, Stuart J, Chen G, Carr A, Seely EW, Fitzmaurice G, Buyandelger Y, Sarantsetseg B, Gantsetseg G, Rich-Edwards J. Randomized trial of three doses of vitamin D to reduce deficiency in pregnant Mongolian women. EBioMedicine. 2019 Jan;39:510-519. doi: 10.1016/j.ebiom.2018.11.060. Epub 2018 Dec 11.
Results Reference
derived

Learn more about this trial

Trial of Vitamin D Supplements to Raise Calcidiol Levels of Pregnant Women in Mongolia

We'll reach out to this number within 24 hrs