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Completed

NCT Number: NCT04082650

Vitamin D and Pregnancy Outcome in PCOS Patients

This multicenter double-blinded placebo-controlled randomised trial aims to evaluate the effectiveness of vitamin D supplementation prior to IVF on the live birth rate in women with PCOS. Women with PCOS scheduled for IVF will be enrolled. Eligible participants will be randomised 1:1 to receive oral capsules of 4000IU vitamin D per day or placebo for around 12 weeks until the day of triggering.

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Key information

Age range

20 year–42 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Peking University Third Hospital, Beijing, Beijing Municipality, China

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About this study

Polycystic ovary syndrome (PCOS) is one of the leading causes of female infertility, affecting around 5% of women with a child-bearing age in China. Vitamin D insufficiency is common in women with PCOS and is associated with lower live birth rates in these women. However, evidence regarding the effectiveness of vitamin D treatment in women with PCOS is inconclusive. This multicenter double-blinded placebo-controlled randomised trial aims to evaluate the effectiveness of vitamin D supplementation prior to IVF on the live birth rate in women with PCOS.

The investigators plan to enroll women with PCOS scheduled for IVF. Eligible participants will be randomised 1:1 to receive oral capsules of 4000IU vitamin D per day or placebo for around 12 weeks until the day of triggering. All IVF procedures will be carried out following a routine method in each center. Women will be followed up until six months after randomisation for those who fail to get pregnant after the completion of the first embryo transfer or delivery for those who get pregnant after the first embryo transfer. The primary outcome is live birth after the first embryo transfer. Primary analysis will be by intention-to-treat analysis. The investigators plan to recruit 860 women to demonstrate women treated with vitamin D have a higher live birth rate than those treated with placebo (48% versus 38%), accounting for 10% loss to follow-up with a significance level at 0.05 and a power of 80%.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women aged 20 to 42 years old;
  • Diagnosed with PCOS (Rotterdam Criteria);
  • Scheduled for IVF;
  • Written informed consent.

Exclusion criteria

  • Women who had three or more failed IVF cycles;
  • Women scheduled for preimplantation genetic testing;
  • Known Vitamin D allergy;
  • Women with a history of chronic absorption syndrome or bile dysplasia, or parathyroid dysfunction, or kidney stones, or blood Calcium ion concentration greater than 2.6mmol/L (normal value 2.25 - 2.75mmol/L (9 to 11mg/dl), or hyperphosphataemia (1.61mmol/L), or metabolic-related bone disease, or chronic diseases that may cause bone abnormalities (liver and kidney insufficiency);
  • Women receiving treatments for tuberculosis, convulsions, and epilepsy because medications treating these diseases may affect the metabolism of vitamin D.
  • Women undergoing an IVF treatment with donor oocytes.

Treatment and study plan

Vitamin D

Drug

4000IU per day

Other names: non

Placebo

Other

The same doses with vitamin D

Primary outcomes

  1. Number of Participants with live birth

    Time frame: 1 day after delivery

    The primary outcome is live birth after the first embryo transfer. Live birth is defined as the delivery of at least one baby after 24 weeks of gestation that exhibits any sign of life.

Secondary outcomes

  1. Number of Participants with Cumulative live birth

    Time frame: 6 months after randomization of the last participant

    Cumulative live birth: defined as live birth resulting from pregnancies that occur within 6 months after randomization.

  2. Number of Participants with Clinical pregnancy

    Time frame: 4 weeks after embryo transfer

    Clinical pregnancy: defined as at least one gestational sac on ultrasound at around 7 weeks' gestation with the detection of heart beat activity after the completion of the first embryo transfer;

  3. birth weight

    Time frame: The day of delivery

    Weight of newborns at delivery.

  4. Number of Participants with miscarriage

    Time frame: 24 gestational weeks in maximum

    miscarriage was defined as a positive pregnancy test but no detectable heart rate before 24 weeks' gestation after the completion of the first transfer;

  5. Number of Participants with Ongoing pregnancy

    Time frame: at 12 weeks' gestation

    defined as pregnancy with detectable heart rate at 12 weeks' gestation or beyond after the completion of the first transfer

  6. Number of Participants with Biochemical pregnancy

    Time frame: 2 weeks after embryo transfer

    defined with a positive pregnancy test

  7. Number of Participants with Ectopic pregnancy

    Time frame: 4 weeks after embryo transfer

    defined as embryo implanted at any site other than the endometrial lining of the uterus cavity after the completion of the first transfer

  8. Number of Participants with Ovarian hyperstimulation syndrome

    Time frame: From the day of oocyte retrieval to two weeks after embryo transfer

    defined according to the Golan criteria. Moderate OHSS is diagnosed by the presence of ascites on ultrasonography in addition to abdominal distension and discomfort with or without nausea, vomiting and/or diarrhea. Severe OHSS is diagnosed when there is clinical evidence of ascites and/or hydrothorax or breathing difficulties with or without hemoconcentration, coagulation abnormalities and diminished renal function.

  9. Number of available embryos for transfer

    Time frame: 5 days after oocyte retrieval

    non

  10. Number of Participants with Pre-eclampsia

    Time frame: 20 weeks of gestation till delivery

    defined as the development of gestational hypertension with proteinuria (≥300 mg/24-hour urine collection or 30 mg/dL in single urine sample) of new onset after 20 weeks of gestation after the completion of the first transfer

  11. Number of Participants with Gestational hypertension

    Time frame: 20 weeks of gestation till delivery

    defined as the development of blood pressure greater than 140/90 mmHg after pregnancy without proteinuria or other signs of preeclampsia after the completion of the first transfer;

  12. Number of Participants with Premature rupture of membrane

    Time frame: The day of delivery

    PROM was defined as rupture of the amniotic membranes before the onset of labor including PROM at term and preterm PROM.

  13. Number of Participants with Postpartum hemorrhage

    Time frame: 1 day after delivery

    defined as the loss of 500 ml of blood or more after completion of the third stage of labor after the completion of the first transfer

  14. Number of Participants with Preterm delivery

    Time frame: 1 day after delivery

    Defined as delivery of a fetus at less than 37 and more than 28 weeks' gestational age after the completion of the first transfer

  15. Number of Participants with Gestational diabetes mellitus

    Time frame: Up to ten months once the participants get pregnancy

    defined as carbohydrate intolerance of variable severity with onset or first recognition during pregnancy as determined from the diagnosis in the obstetrical medical record

  16. Number of Participants with Placenta previa

    Time frame: after 24 weeks of gestation

    defined as a placenta that is implanted over or very close to the internal cervical orifice

  17. Number of Participants with Stillbirth

    Time frame: 1 day after delivery

    defined as the absence of signs of life at or after birth after the completion of the first transfer

  18. Apgar score

    Time frame: 1 minute or 5 minutes after delivery

    non

  19. Serum Vitamin D binding protein, glucose, insulin, Calcium ion concentration

    Time frame: The day of oocyte retrieval

    non

  20. Serum vitamin levels

    Time frame: One day before oocyte retrieval

    Serum vitamin levels at the triggering day

Sponsors and collaborators

Lead sponsor

Women's Hospital School Of Medicine Zhejiang University

Other

Registry information

Official study title

Vitamin D Supplementation Prior to in Vitro Fertilization in Women With Polycystic Ovary Syndrome: a Protocol of a Multicenter Randomised Double-blind Placebo-controlled Clinical Trial

Important dates

Study start
2020
Primary completion
2024
Study completion
2025
First posted
Sep 9, 2019
Registry last updated
Jan 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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