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The impact of vaginal progesterone and vitamin D3 on the treatment of unexplained recurrent abortion

Effect of concomitant administration of vaginal progesterone and vitamin D3 in the treatment of unexplained recurrent abortion in pregnant women

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013100114853N1
Enrollment
80
Registered
2013-10-30
Start date
2013-11-22
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Recurrent abortion. spontaneous abortion

Interventions

Intervention 1: control group: Participants are treated with 400 mg vaginal progesterone suppositories (manufactured by Behvazan Pharmaceutical company, Iran) at a dose of 400 mg/day until the 20th we
Treatment - Drugs
control group: Participants are treated with 400 mg vaginal progesterone suppositories (manufactured by Behvazan Pharmaceutical company, Iran) at a dose of 400 mg/day until the 20th week of pregnancy.
control group: Participants are treated with vaginal progesterone suppositories at a dose of 400 mg/day manufactured by Behvazan Pharmaceutical company, Iran, and vitamin D3 at a dose of 4000 IU/day (

Sponsors

Vice Chancellor for research, Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Incidence of 3 or more consecutive recurrent abortions or 2 or more non consecutive abortions; Age less than 35 years and above 18 years; The absence of any known causes of abortion; Pregnancies from one single husband in previous and current abortions Exclusion criteria: Uterine anomalies; The history of allergy on the consumption of progesterone and multivitamins containing vitamin D3; initial abnormal tests of thyroid abnormalities, prolactin, antiphospholipid antibody syndrome and thrombophilia

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Continuation of pregnancy beyond 20 weeks of pregnancy in women with recurrent abortion. Timepoint: 20 weeks after the first day of last menstural period. Method of measurement: clinical, laboratory and sonographic findings.

Secondary

MeasureTime frame
Continuation of pregnancy. Timepoint: after pregnancy termination. Method of measurement: after pregnancy termination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFarzaneh Amini

Department of Obstetrics and Gynecology, Kashan Medical School

amini-si@kaums.ac.ir+98 36 1446 0180

Outcome results

None listed

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