What will my patient's participation involve once she provides consent?

Your patient's participation in the observational pregnancy study may last throughout her pregnancy and up to one year after her delivery date. Your patient will be contacted once per trimester, at the estimated date of delivery, and when her infant is 3, 6, 9, and 12 months of age to provide basic information about her pregnancy, post pregnancy health and her infant's health. At each timepoint your patient will be asked to confirm her contact information.

After my patient provides consent, what will my participation involve?

A healthcare provider's (HCP) participation will vary depending on if they are treating the patient or infant. The woman's obstetric HCP will be contacted between the 6th and 7th month of the patient's pregnancy and, again, within 4 weeks after the estimated delivery date. The pediatric HCP will be contacted when the baby is approximately 3, 6, 9, and 12 months old. In order to collect the information, The Pregnancy Coordinating Center will send questionnaires to the appropriate HCP for completion.

How will the data be collected?

The Pregnancy Coordinating Center is responsible for collecting the study data. All data provided by you and/ or your patient will be entered into the study database. The study database will be kept on a secure computer system maintained by the study administrator in accordance with their written security policy. Information about your health collected while you are in the Lampit^® Pregnancy Registry will be kept anonymous and any identifying information will not be used.

The success of the pregnancy registry depends on the continued participation of healthcare providers like you. We greatly appreciate your help with identifying pregnancies, and in assisting with the collection of follow-up information during your patient's participation in the study.