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Does Valproate Increase Levels of Folate Receptor Autoantibodies in Women?

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Northwell Health

Status

Completed

Conditions

Epilepsy
Psychiatric or Mood Diseases or Conditions

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT01231646
10-266A

Details and patient eligibility

About

Women who take folate (folic acid) before getting pregnant can lower the risk of giving birth to infant with certain birth defects. However, some medications may affect the action of folate. The purpose of this study is to compare the effect of two anti-epileptic drugs on how folate works in our body.

Enrollment

38 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Women ages 18-50 years inclusive who are taking valproate or lamotrigine for neurologic or psychiatric conditions
  • Valproate of lamotrigine must be used as monotherapy at stable doses for 6 weeks prior to the study for the neurologic or psychiatric illness; medications taken for other reasons are not excluded.

Exclusion criteria

  • Women with prior exposure to valproate or lamotrigine if they are taking lamotrigine or valproate respectively.

Trial design

38 participants in 2 patient groups

Lamotrigine
Description:
No intervention
Treatment:
Other: No intervention
Valproate
Description:
No intervention
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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