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Recruiting NCT05754593

Study of Ovarian Reserve Concerning Patients With Multiple Sclerosis (MS), Compared to a Control Group

No phase Interventional Multiple Sclerosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Anti-Mullerian hormone (AMH) level, Antral follicle count (AFC), Clinical assessment.
Who it may be relevant to
Registry conditions: Multiple Sclerosis. Basic parameters: 25 years — 35 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Study of Ovarian Reserve Concerning Patients With Multiple Sclerosis, Compared to a Control Group

Overview

The investigators want to evaluate ovarian reserve concerning patients with multiple sclerosis, compared to a control group of healthy women. This study will include women from 25 to 35 years old.

Detailed description

Multiple sclerosis is an inflammatory disease of central nervous system, with a prevalence rate in France of 1 case/1000 subjects. The average age at diagnosis is 30 years old and it affects especially women, with a sex ratio of 3 women for 1 men. Multiples sclerosis concerns women at a moment when fertility is a main issue.

Few studies suggest that there is an negative impact of multiple sclerosis on ovarian reserve, with a combined mechanism ( inflammatory and autoimmune mechanism). The investigators can hypothesize that patients with multiple sclerosis are more predisposed to have primary ovarian insufficiency.

Ovarian reserve is evaluated by Anti-Mullerian Hormone (AMH) dosage and antral follicle count (AFC) by ultrasound imaging.AMH levels can be measured at every moment of the menstrual cycle whereas AFC is preferentially performed between the second and the eighth day of the menstrual cycle. The combined use of this two markers is well known to be correlated with ovarian reserve. Only a few studies have evaluated ovarian reserve in patients with multiple sclerosis. Besides, there is only a few number of participants and results are contradictory. A decrease of ovarian reserve identified among patients with multiple sclerosis could lead to an orientation in a fertility preservation center.

This project is a monocentric study realized at Pellegrin Hospital - Bordeaux. Patients with multiple sclerosis belong to a cohort of the neurology center. Healthy women come from a volunteer base contacted by email.The two groups are matched thanks to answers of a short questionnaire.Measure of AMH level is performed at pellegrin Hospital at the medical laboratory. Ultrasound imaging is performed by the center of women imagery at Pellegrin Hospital. Results are communicated by teleconsultation two months later. If there is an anormal result, a specific appointment will be organized with a gynecologist.

Interventions

  • Biological Anti-Mullerian hormone (AMH) level
    Measure of Anti-Mullerian hormone (AMH) level by blood sample
  • Other Antral follicle count (AFC)
    Measure of Antral follicle count (AFC) by ultrasound imaging
  • Other Clinical assessment
    MS history and MS treatments and Expanded Disability Status Scale (EDSS) score will be recorded

Primary outcome measures

  • Measure of Anti-Mullerian hormone (AMH) level by blood sample to compare ovarian reserve between patients with multiple sclerosis versus healthy controls from 25 to 35 years old. [Time frame: At baseline (day 0)]
Secondary outcome measures (1)
  • Measure of Antral follicle count (AFC) by ultrasound imaging to compare ovarian reserve between patients with multiple sclerosis versus healthy controls from 25 to 35 years old. [Time frame: At baseline (day 0)]

Eligibility criteria

Inclusion criteria

  • Reproductive women between 25 and 35 years old ;
  • MS Patient : Diagnosis of multiple sclerosis based on McDonald Criteria 2017;
  • French-speaking, without comprehension disorders ;
  • being affiliated to health insurance ;
  • Willing to participate and to sign informed consent.

Exclusion criteria

  • History of ovarian surgery (cystectomy, annexectomy) ;
  • Turner Syndrome ;
  • fragile X messenger ribonucleoprotein 1 (FMR1) premutation ;
  • Endometriosis with a risk of ovarian reserve alteration ;
  • History of chemotherapy or pelvic radiotherapy ;
  • Pregnant or breastfeeding women ;
  • patient concerned by articles L 1121-5 to L 1121-8 (persons deprived of their liberty by a judicial or administrative decision, minors, persons of legal age who are the object of a legal protection measure or unable to express their consent).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

France · 1 center
  • CHU de Bordeaux - service de neurologie — Bordeaux

Identifiers

NCT: NCT05754593 · CHUBX 2022/27

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗