Pregnant Women with Neuroimmune Diseases: A long-term follow-up study
Official title: Cohort Study on Neuroimmune Diseases in the Reproductive Age
Run by Third Affiliated Hospital, Sun Yat-Sen University · NCT07653984 · Data updated 2026-11-12
This study follows women with neuroimmune diseases and healthy controls through pregnancy and up to ten years to see how pregnancy affects disease activity and outcomes for both mother and baby.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 20 Years to 55 Years |
| Sex | Women only |
| Enrollment | 100 (estimated) |
| Sponsor | Third Affiliated Hospital, Sun Yat-Sen University Academic / other |
| Locations | 1 site (Guangzhou, Guangdong) |
| Status | Recruiting |
| Started | April 21, 2024 |
| Main results expected | January 2030 |
| Study ends | April 2030 |
| Registry record updated | June 17, 2026 |
| Trial ID | NCT07653984 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Women aged 20-55 with a confirmed neuroimmune diagnosis or healthy, age-matched controls planning pregnancy.
✕Probably not a fit
Patients with undetermined diagnoses, incomplete data, or those who withdraw consent may not benefit from the findings.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study tracks 50 women of childbearing age with NMOSD, MS, autoimmune encephalitis, myasthenia gravis, GBS, or MOGAD, plus 50 healthy controls, to observe relapse rates, symptoms, imaging, treatments, and blood profiles during pregnancy and postpartum. Data include EDSS scores and MRI results, maternal drug levels, and neonatal development, with a plan for extended follow-up up to ten years. The primary aim is to generate detailed clinical data to help clinicians optimize disease management during pregnancy and after delivery. Enrollment prioritizes voluntary consent and complete personal information, with geographic restriction to a single Chinese center. The study is observational and does not specify a treatment intervention.
Why it matters
Potential benefit: If successful, the study could provide evidence-based guidance for managing neuroimmune diseases during pregnancy to improve maternal and neonatal outcomes.
How similar studies have gone: Other observational studies have explored pregnancy and autoimmune neuroinflammatory conditions, but this study’s long-term ten-year follow-up and inclusion of MOGAD provide additional, less-explored data.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient Group: A total of fifty participants are expected to be enrolled. 1. Women aged 20-55 years with childbearing potential. 2. Voluntary informed consent. 3. Availability of complete personal information. 4. A confirmed diagnosis of neuromyelitis optica spectrum disorder (NMOSD), multiple sclerosis (MS), autoimmune encephalitis, myasthenia gravis, Guillain-Barré syndrome, or myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD). Healthy Control Group: A total of fifty healthy women are expected to be included. 1. Age- and sex-matched women of childbearing age with plans for pregnancy 2. Voluntary informed consent. 3. Availability of complete personal information. Exclusion Criteria: * Patient Group: 1. Patients with an undetermined or unconfirmed diagnosis. 2. Incomplete personal information that cannot be obtained through follow-up. 3. Participants who voluntarily withdrew from the study and revoked informed consent. Healthy Control Group: 1. Individuals diagnosed with neuroimmune-related disorders. 2. Incomplete personal information that cannot be obtained through follow-up. 3. Participants who voluntarily withdrew from the study and revoked informed consent.
Where it's running
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The Third Affiliated Hospital, Sun Yat-sen University
Guangzhou, Guangdong, China Recruiting
Study contacts
- Study coordinator: Wei Qiu, Ph.D
- Email: qiuwei120@vip.163.com
- Phone: 15899968330
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.