Fampridine Pregnancy Exposure Registry

Status Terminated

Clinical Trial Summary

This is a global pregnancy registry to evaluate the outcomes of pregnancy in women with multiple sclerosis who have been exposed to prolonged-release fampridine since the first day of their last menstrual period prior to conception or at any time during pregnancy.

Clinical Trial Description

There are no mandatory physician visits. The registry will collect pregnancy outcome data from the participants health care provider during the prenatal follow up (6-7 months gestation), pregnancy outcome (4 weeks after estimated delivery date) and finally the pediatric follow up (at 4 weeks and 12 weeks post birth). ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01532154
Study type	Observational [Patient Registry]
Source	Biogen
Contact
Status	Terminated
Phase	N/A
Start date	August 2015
Completion date	February 2016

View Details

See also
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