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Clinical Trial Summary

The purpose of the study is to develop a detailed pregnancy registry of patients with Multiple Sclerosis in the New England states. Women with a diagnosis of MS that are either pregnant or actively planning to become pregnant are eligible to participate. The study will solely take place through phone interviews. One of the study coordinator at the Partners MS Center will contact the participant for an intake phone interview where general information about the individual, their pregnancy and their MS will be collected. Thereafter the coordinator will contact the participant every 3 months for 20 minutes follow up interviews. After birth, the coordinator will collect information on the growth and development of the participant's baby. Pediatric interviews will be conducted at 2, 4, 6, 9, 12, 18, 24, 36 months. Information from the participant's neurologist and obstetrician, as well as information from the baby's pediatrician, will be made available to the study staff at regular intervals throughout the duration of the study. Through this study, the investigators hope to learn more about the effects of MS on pregnancy and pediatric development, and about the effects of pregnancy on the course of MS.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03368157
Study type Observational
Source Brigham and Women's Hospital
Contact Maria K Houtchens, M.D.
Phone 6175256550
Email mhoutchens@bwh.harvard.edu
Status Recruiting
Phase
Start date April 7, 2017
Completion date December 7, 2022

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