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A randomized controlled clinical trial of vitamin D supplementation during perinatal pregnancy to reduce recurrent abortion in patients with recurrent pregnancy loss

Clinical trial of vitamin D supplementation during perinatal pregnancy to reduce recurrent abortion in patients with recurrent pregnancy loss

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091656
Enrollment
Unknown
Registered
2024-10-31
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

recurrent pregnancy loss

Interventions

Study group:According to the current routine treatment of recurrent abortion, the study group was given the corresponding treatment, at the same time, vitamin D drops were given 2000IU /d. 25-hydroxyv
Control group:The control group was given the corresponding treatment according to the current routine of recurrent abortion, and was given 400IU /d vitamin D drops until 28 weeks of pregnancy or anot

Sponsors

Shanghai First Maternity and Infant Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
19 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) Aged 19 - 40years 2) Two or more miscarriages with the 28th gestational week 3) peripheral blood 25-hydroxyvitamin D level <30ng/L (75nmol/L) 4) Planning to be pregnant or pregnancy within 7 gestational weeks 5) Voluntarily participating in this study and signing an informed consent form.

Exclusion criteria

Exclusion criteria: 1) Parental karyotype abnormalities (Chromosomal balanced translocation or Robertsonian translocations) 2) Genital tract abnormalities 3) Combine hyperprolactinemia that has not been treated, thyroid dysfunction that has not been treated, poorly controlled diabetes, and uncontrolled hypertension that has not been treated according to guidelines. 4) Serious primary diseases of liver, kidney, heart, lung and other organs are not suitable for pregnancy or other pregnancy contraindication5) Patients with kidney stones, chronic constipation 4) Allergy to vitamin D preparations

Design outcomes

Primary

MeasureTime frame
Spontaneous Abortion rate;

Secondary

MeasureTime frame
Gestational diabetes mellitus ;Preeclampsia;preterm birth; small for geatational age;Iive birth rate;

Countries

China

Contacts

Public ContactGuohua Li

Shanghai First Maternity and Infant Hospital,

yuhuashi1979@163.com+86 135 6426 9395

Outcome results

None listed

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