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Pregnancy Cohort in Multiple Sclerosis (MS)

Pregnancy Cohort in Multiple Sclerosis (MS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05010902
Enrollment
100
Registered
2021-08-18
Start date
2013-01-01
Completion date
2026-12-31
Last updated
2024-07-05

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

Conditions

Clinically Isolated Syndrome (CIS), Multiple Sclerosis (MS)

Keywords

Pregnancy

Brief summary

Multiple sclerosis (MS) is a common inflammatory demyelinating disorder of the central nervous system frequently affecting females in their reproductive phase of life. In this prospective observational study, we obtain data on the outcome of pregnancies in MS patients and the influence of pregnancy on clinical, laboratory and MRI parameters in MS.

Interventions

None listed

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* age \> 18 years * signed informed consent * diagnosis of multiple sclerosis or clinically isolated syndrome

Exclusion criteria

* clinically relevant comorbidities * contraindications for MRI, e.g. pacemaker, metal implants, allergy against gadolinium * alcohol or drug abuse

Design outcomes

Primary

MeasureTime frameDescription
Time until relapse12 months after delivery compared to baselineTime (in days) until relapse during the observation period

Secondary

MeasureTime frameDescription
Number of T2 lesions12 months after delivery compared to baselineNumber of T2 lesions in spinal and cerebral magnetic resonance imaging
Number of gadolinium enhancing lesions12 months after delivery compared to baselineNumber of gadolinium enhancing lesions in spinal and cerebral magnetic resonance imaging
Volume of T2 lesions12 months after delivery compared to baselineVolume of T2 lesions in spinal and cerebral magnetic resonance imaging
Volume of gadolinium enhancing lesions12 months after delivery compared to baselineVolume of gadolinium enhancing lesions in spinal and cerebral magnetic resonance imaging
Change in immune cell phenotypes12 months after delivery compared to baselineChange in immune cell phenotypes of peripheral blood mononuclear cells (PBMC)
Galectin-112 months after delivery compared to baselineChange in serum galectin-1 concentration measured by ELISA
Galectin-312 months after delivery compared to baselineChange in serum galectin-3 concentration measured by ELISA
Galectin-912 months after delivery compared to baselineChange in serum galectin-9 concentration measured by ELISA
Neurofilament (NfL)12 months after delivery compared to baselineChange in neurofilament serum concentration by using Simoa NfL assay
Anti-inflammatory interleukin-1012 months after delivery compared to baselineChange in anti-inflammatory interleukin-10 serum concentration assessed by ELISA
Autoantibody profiling12 months after delivery compared to baselineIdentification and quantification of autoantibodies by using protein microarray and ELISA
Pro-inflammatory interleukin-1712 months after delivery compared to baselineChange in interleukin-17 serum concentration assessed by ELISA
Thickness of the retinal nerve fibre layer12 months after delivery (compared to baseline)Thickness of the retinal nerve fibre layer by Optical Coherence Tomography (OCT)
Total macular volume (TMV)12 months after delivery compared to baselineTotal macular volume by Optical Coherence Tomography (OCT)
Mini-International Neuropsychiatric Interview (M.I.N.I.) German Version 5.0.0 Module A-C12 months after delivery compared to baselineStructured diagnostic interview to assess depression, dysthymia and suicidality
Montgomery-Asberg Depression Rating Scale (MADRS)12 months after delivery compared to baselineRating of ten depression related symptoms on a scale from 0 to 6 (higher numbers indicate more severe symptoms)
Beck Depression Inventory (BDI-II)12 months after delivery compared to baselineRating of 21 depression related symptoms on a scale from 0 to 3 (higher numbers indicate more severe symptoms)
Edinburgh Postpartum Depression Scale (EPDS)12 months after delivery compared to baselineSelf-report survey containing 10 items, each item is rated 0-3 (higher scores indicate a higher probability of postpartum depression)
Modified Fatigue Inventory Scale (MFIS)12 months after delivery compared to baselineSelf-report survey containing 21 items, each item is rated 0-4 (higher scores indicate a greater impact of fatigue on a person's activities)
Fatigue Severity Scale (FSS)12 months after delivery compared to baselineA self-report survey consisting of 11 items, each item ranges from 1 to 7 (higher scores indicate higher levels of fatigue)
Visual Fatigue Analogue Scale (VFAS)12 months after delivery compared to baselineA self-administered, single scale indication measuring visual fatigue, ranging from 0 to 100 (higher scores indicate worse fatigue)
Short-Form Health Survey (SF-36)12 months after delivery compared to baselineA self-report survey measuring health in eight dimensions (higher scores indicate less disability)
Fecal microbiome composition12 months after delivery compared to baselineComposition of fecal microbiome measured by 16S Sequencing

Countries

Germany

Contacts

Primary ContactNadja Siebert, MD
nadja.siebert@charite.de
Backup ContactFriedemann Paul, Prof.
friedemann.paul@charite.de

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026