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Effect of hydroxychloroquine on recurrent abortion treatment

Assessment the effect of hydroxychloroquine on the treatment of unexplained recurrent abortion in women referred to Arash hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2015120910664N2
Enrollment
60
Registered
2016-07-18
Start date
2016-06-21
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: intervention group: After confirming the positive pregnancy test, patients will receive tablet of 200 mg hydroxychloroquine twice a day up to the twentieth week of pregnancy.Sonography
Treatment - Drugs
intervention group: After confirming the positive pregnancy test, patients will receive tablet of 200 mg hydroxychloroquine twice a day up to the twentieth week of pregnancy.Sonography will be done in
control group: After confirming the positive pregnancy test, patients will receive placebo twice a day up to the twentieth week of pregnancy.Sonography will be done in weeks of 6-8, 11-13 and 18-22 of

Sponsors

Experimental Medicine Research Centerof Tehran University of Medical Science,Vice chancellor for res
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: inclusion criteria : women with more than 2 unexplained abortion exclusion criteria: women with rheumatoid; lupus erythematosus; underlying and heart diseases; smoking; consumption of alcohol and supplement; radiation contact

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Spontaneous abortion. Timepoint: any time during study. Method of measurement: observational.

Secondary

MeasureTime frame
Intrauterine death. Timepoint: after 20 weeks of gestation. Method of measurement: observational.;Preeclampsia. Timepoint: all the duration of pregnancy. Method of measurement: clinical and laboratory examination.;Low birth weight. Timepoint: after birth. Method of measurement: weighing.;Preterm labor. Timepoint: before 37 th week of gestation. Method of measurement: observational.;Congenital morphological abnormalities. Timepoint: after birth. Method of measurement: observational.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Reihaneh Pirjani

Arash Women 's Hospital, Tehran University of Medical sciences

pirjani@razi.tums.ac.ir+98 21 7788 3196

Outcome results

None listed

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