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OpenTrials
Completed

NCT Number: NCT04228263

Hydroxychloroquine and Unexplained Recurrent Miscarriage

Recurrent miscarriage affects women of childbearing age worldwide. Vascular endothelial dysfunction and immunological impairment are associated with recurrent miscarriage To date, there is no effective or optimal therapeutic approach for these condition. Hydroxychloroquine has endothelial protective action via ant diabetic, lipid lowering, antioxidant effects or direct endothelial protection. Hydroxychloroquine is an antimalarial and immunomodulatory agent. In pregnancy, hydroxychloroquine is prescribed for inflammatory conditions associated with adverse perinatal outcomes such as systemic lupus erythematosus, antiphospholipid syndrome and placental inflammatory lesions such as chronic histiocytic intervillositis, hydroxychloroquine has therapeutic potential to improve placental function in pregnancies associated with heightened inflammation.

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Key information

Age range

20 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Abdel-rahman Mahmoud Mohammed

Asyut, 71111, Egypt

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Women aged between 20- 40 years inclusive. 2. Body Mass Index (BMI) between 18.5 -35 Kg/m2 3. Had at least 2 previous miscarriage before 20 weeks 4. Women willing to conceive. 5. Regular Ovulatory cycles. 6. No anatomical or endocrine cause of recurrent pregnancy loss. 7. Women who have given their informed consent. 8. Negative antibody test for antiphospholipid syndrome (Lupus anticoagulant, Anticardiolipin IgM, IgG, B2glycoprotein) Exclusion criteria
  • Women who are already pregnant.
  • Known contraindication to a treatment by HCQ (retinopathy, hypersensitivity to chloroquine or HCQ, G6PD deficiency, acute intermittent porphyria, chronic liver or kidney insufficiency, extensive cutaneous psoriasis not controlled by local treatment, significant chronic digestive , hematologic disease epilepsy or psychotic disorders.) or known rare disorder of lactose metabolism .
  • Patient already using HCQ
  • Patient not get pregnant after 12 months of HCQ use.

Treatment and study plan

Hydroxychloroquine

Drug

400mg

Folic Acid

Drug

5 mg

Low-dose aspirin

Drug

75 mg

Primary outcomes

  1. Number of viable fetuses at 20 weeks gestation

    Time frame: 5 months

Secondary outcomes

  1. Number of patients with miscarriage before 20 weeks

    Time frame: 5 months

  2. Number of pregnancy complications such as ( FGR or preeclampsia, IUFD after 20 week gestation)

    Time frame: 9 months

  3. Number of fetus with Major congenital anmalies

    Time frame: 9 months

  4. Number of Live birth

    Time frame: 9 months

  5. Number of Preterm delivery before 37 week gestation.

    Time frame: 8 months

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Official study title

Hydroxychloroquine for Improvement of Pregnancy Outcome in Unexplained Recurrent Miscarriage

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Jan 14, 2020
Registry last updated
Dec 7, 2023

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.