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Effect of supplementation in treatment of women with gestational diabetes

Clinical trial of the effect of multi mineral-vitamin D supplementation compared with the placebo on pregnancy outcomes in women with gestational diabetes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201704225623N109
Enrollment
60
Registered
2017-04-25
Start date
2017-03-01
Completion date
Unknown
Last updated
2019-11-05

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

Conditions

Gestational diabetes. Diabetes mellitus in pregnancy, unspecified

Interventions

Intervention 1: Intervention group: Multi mineral-vitamin D supplements (Vitane, Wolfratshausen, Germany), 400 mg calcium, 100 mg magnesium, 4 mg zinc, 200 IU vitamin D3, daily, for 6 weeks orally. In

Sponsors

Vice chancellor for research, Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: Pregnant women aged 18-40 years Diagnosed with GDM at 24-28 weeks' gestation

Exclusion criteria

Exclusion criteria: History of placenta abruption Pre-eclampsia Eclampsia Hypo and hyperthyroidism Kidney or liver diseases Taking magnesium, zinc, calcium and vitamin D supplements prior to intervention Being smoker Insulin therapy after GDM diagnosis

Design outcomes

Primary

MeasureTime frame
Hs-CRP. Timepoint: At the beginning of the study and after 6 weeks of intervention. Method of measurement: ELISA kit.;Total nitrite. Timepoint: At the beginning of the study and after 6 weeks of intervention. Method of measurement: Spectrophotometry.

Secondary

MeasureTime frame
Total antioxidant. Timepoint: At the beginning of the study and after 6 weeks of intervention. Method of measurement: Spectrophotometry.;Malondialdehyde. Timepoint: At the beginning of the study and after 6 weeks of intervention. Method of measurement: Spectrophotometry.;Glutathione. Timepoint: At the beginning of the study and after 6 weeks of intervention. Method of measurement: Spectrophotometry.;Newborn length. Timepoint: The first 24 h after birth. Method of measurement: Scale.;Newborns' weight. Timepoint: The first 24 h after birth. Method of measurement: Scale.;Polyhydramnios. Timepoint: After the intervention. Method of measurement: Sonography.;Newborn's head circumference. Timepoint: Delivery time. Method of measurement: Tape.;Newborn's bilirubin. Timepoint: Delivery time. Method of measurement: Enzymatic kit.;Apgar score. Timepoint: Delivery time. Method of measurement: Clinical observation.;Preterm delivery. Timepoint: After delivery. Method of measurement: Medical record.;Maternal pre-eclampsia. Timepoint: After delivery. Method of measurement: Medical record.;Maternal hospitalization. Timepoint: After delivery. Method of measurement: Medical record.;Newborns' hospitalization. Timepoint: After delivery. Method of measurement: Medical record.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZatollah Asemi

Kashan University of Medical Sciences

asemi_z@kaums.ac.ir+98 31 5546 3378

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 21, 2026