Néevo®/NéevoDHA® P.L.U.S. Program (Progress Through Learning, Understand & Support)

Stopped early

Conditions studied: Pregnancy

In brief

This is an observational study in which patients who have been prescribed Néevo®/NéevoDHA® are invited to participate in surveys about their pregnancy and experiences with Néevo®/NéevoDHA®. The purpose of this study is to increase the understanding of the role of L-methylfolate among patients who are candidates for Néevo®/NéevoDHA®, provide patients with personalized education and support during their pregnancies, and contribute to the overall understanding of the needs and concerns of women facing intermediate- to high-risk pregnancies.

Key facts

Study ID

NCT01358552

Run by

Pamlab, Inc.

People needed

53

Starts

2011-01-01

Expected to finish

2012-03-01

Last updated by the study team

2013-05-01

Who can join

Age: 18 and older, up to 39. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• New Néevo®/NéevoDHA® Start.
• Only for women who are pregnant and taking brand name Néevo®/ NéevoDHA® under a physicians care.

You may not qualify if…

• Patients who are not pregnant.
• If participant indicates that she did not get a prescription for Néevo®/ NéevoDHA®, she will not be able to complete the survey(s).
• For the follow-up survey, if the participant indicates that she has not been taking Néevo®/NéevoDHA®, she will not be able to complete the survey( (s).

Where it is running

• Noe Lira, M.D. — Corpus Christi, Texas, United States

Full record on ClinicalTrials.gov

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