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The effect of an additional dose of vitamin D3 supplementation on the rate of cessation and recurrence of preterm labor in women referred to the hospital

The effect of an additional dose of vitamin D3 supplementation on the rate of cessation and recurrence of preterm labor in women referred to the hospital

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240111060683N1
Enrollment
68
Registered
2024-02-12
Start date
2024-02-10
Completion date
Unknown
Last updated
2024-03-06

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

Conditions

The effect of an additional dose of vitamin D3 supplement on the rate of cessation and recurrence of premature labor in women referred to Bahlul Gonabad and Vali Asrbirjand hospitals 1402. Preterm labor

Interventions

Intervention 1: In the intervention group, an additional dose of 1000 units of vitamin D (2000 units in total) will be prescribed to the intervention group for a maximum of one week after the onset of

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
10 Years to 56 Years

Inclusion criteria

Inclusion criteria: Vitamin D serum level less than 32 ng Willingness to participate in the study Age range 10-54 years Gestation age 24 to 36 weeks and 6 days Not having pregnancy complications based on the mother's statement or information in the mother's file (multiple twins, polyhydramnios, preeclampsia, uncontrolled diabetes, uncontrolled hypothyroidism) that causes premature birth. No rupture of the water bag Dilatation of less than 3 centimeters and defecation Failure to perform cerclage and history of cerclage Absence of urinary infection and vaginal infection during pregnancy based on the mother's statement or the information in the mother's file

Exclusion criteria

Exclusion criteria: The mother's unwillingness to cooperate to take a blood sample Mother's unwillingness to continue studying Occurrence of intrauterine fetal death

Design outcomes

Primary

MeasureTime frame
The number of people who gave birth prematurely (before 37 weeks of pregnancy). Timepoint: Before the intervention and one week after the intervention. Method of measurement: Follow-up of mothers and that their delivery was in several weeks of pregnancy.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSomayeh Khajeh

Gonabad University of Medical Sciences

smyhkhwajh@gmail.com+98 915 562 4250

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026