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.
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 Type
OBSERVATIONAL
Enrollment
1
As prescribed and taken after the last menstrual period prior to becoming pregnant or anytime during the pregnancy
Hopital Pitie Salpetriere
Paris, France
Spontaneous abortions
Time frame: < 22 weeks of gestation
Elective or therapeutic terminations
Time frame: Up to 9 months of pregnancy
Ectopic pregnancy
Time frame: Up to 9 months of pregnancy
Fetal death including still births
Time frame: >22 weeks of gestation or weighing 500 grams
Live born infants
Time frame: During delivery time ( at expected average 9 months of pregnancy)
Premature births
Time frame: Delivered before 37 Weeks of gestation
Maternal death
Time frame: During pregnancy, labor or delivery
Neonatal death
Time frame: Prior to 28 days of life
Birth Defects
Time frame: Delivery time (expected 9 months of pregnancy)
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