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Recruiting Phase 1

Treatment and Clinical Outcomes Among SLE Patients in Pregnancy

NCT04976465 · tracked via the Priya Life Science China tracker
Phase
Phase 1
Started
2018-01-01
Last updated
2023-11-18

Condition(s) studied

Systemic Lupus ErythematosusPregnancy Related

Investigational drug(s) / intervention(s)

AnticoagulationWithout Anticoagulation

Anticoagulation: Drug: 1. Prednisone 5-30mg, po, once per day(Qd) prescribed if needed and adjusted due to patient response Other Names: Pred 2. Hydroxychloroquine 100-200mg, po, twice per day (Bid) prescribed if needed and adjusted due to patient response. Other Names: HCQ 3. Aspirin 100mg, po, once per day (Qd) prescribed if needed and adjusted due to patient response to 32 weeks of pregnancy. 75mg po, once per day (Qd) to 34 weeks of pregnancy. 50mg po, once per day (Qd) to 36 weeks of pregnancy. Other Names: Asp 4. Low molecular weight heparin Enoxaparin 40-60mg, ih, Subcutaneous injection, once per day (Qd) or twice per day (Bid) if needed and adjusted due to patient response. Other Names: LMWH

Without Anticoagulation: Drug: 1. Prednisone 5-30mg, po, once per day(Qd) prescribed if needed and adjusted due to patient response Other Names: Pred 2. Hydroxychloroquine 100-200mg, po, twice per day (Bid) prescribed if needed and adjusted due to patient response. Other Names: HCQ

Study summary

Systemic lupus erythematosus (SLE) is a kind of systemic autoimmune disease which can cause multiple organs and system damage, which often occurs in women of childbearing age. Compared with healthy pregnant women, SLE patients have higher incidence of premature delivery, preeclampsia and fetal loss during pregnancy. Since SLE patients usually have disease activity during pregnancy and postpartum, and a variety of maternal and fetal diseases are closely related to SLE, it is very important to monitor the disease activity and drug treatment of SLE patients during pregnancy.

Eligibility

Sex
FEMALE
Min age
20 Years
Max age
45 Years
Healthy volunteers
No
Inclusion Criteria: 1. Patients diagnosed with systemic lupus erythematosus (SLE) (ACR criteria, 1997); 2. Pregnant women aged 20-45 years old; 3. Willing to participate in this study, willing to medication and follow-up according to the treatment plan, and sign the informed consent. Exclusion Criteria: 1. The cause of previous abortion was known: * Known chromosomal abnormalities in the parent, maternal or embryo. \- Page 3 of 4 \[DRAFT\] -• Endocrine dysfunction of pregnant women: luteal dysfunction; Polycystic ovarian syndrome; Ovarian premature failure (FSH ≥ 20uu/ L) in follicular stage; * Hyperprolactinemia thyroid disease; Other hypothalamic pituitary adrenal axis abnormalities in diabetes mellitus. * Abnormal anatomy of pregnant women: abnormal uterus; Asherman syndrome; The uterine fibrosis of cervical insufficiency is more than 5 cm. Vaginal infection. * Any known serious heart disease, liver, kidney, blood or endocrine disease. 2. Any active infection Active viral hepatitis includes hepatitis B virus (HBV), hepatitis C virus (HCV), human papillomavirus (HPV). Active infections include small intestine herpes zoster virus (VZV), human immunodeficiency virus (HIV), syphilis or tuberculosis. 3. Allergic to prednisone, hydroxychloroquine, low molecular weight heparin or aspirin. 4. The history of the disease is as follows: * There was a history of peptic ulcer or upper gastrointestinal bleeding in the past. * The past history of malignant tumor. * The past history of epilepsy or psychosis. 5. Women who disagree or cannot complete the follow-up during pregnancy and after delivery.

Primary outcome measure(s)

  • Live birth rate — After 28 weeks of gestation]
    Percentage of all patients that lead to live birth after 28 weeks of gestation

Trial sites (1)

FacilityCityRegionStatus
Qilu Hospital Jinan Shandong Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04976465 on ClinicalTrials.gov ↗ ← All trials in China