A proposed patient education and care-navigation layer for Materna Medical’s pelvic-health portfolio—from Milli at home to the investigational Ellora System in labor and delivery.
A proposed Ema experience could help people find clear, Materna-approved information and reach the right care or study contact—without replacing clinical judgment.
Plain-language education about common pelvic-health concerns and questions to discuss with a clinician.
Help patients navigate approved product information about Milli, its use, and where to find support.
Explain the investigational Ellora System and direct study questions to the appropriate research team.
Offer a clear next step for care-team questions, study information, or follow-up—within an agreed workflow.
A Materna-specific experience should be grounded in approved product and study information, with clinical review and clear routes to human support.
Uses Materna-approved education about pelvic health, Milli, Ellora, and the EASE study.
Sets firm boundaries around medical advice and directs personal care questions to a qualified clinician or study team.
Uses a supportive, respectful voice that reflects Materna’s focus on women’s pelvic health.
Materna’s commercial and investigational products address different needs and stages of care. Any Ema experience should make those distinctions explicit.
Sources: Materna Medical and the Mayo Clinic EASE study listing (NCT03973281). Mayo’s listing calls the device Materna Prep; Materna’s current site describes Ellora. Ellora is investigational; study status can change.
A significant need with no standardized preparation approach.
Broad language capability, limited to an agreed Materna-approved content base.
Applies Materna’s approved product and study information, plus agreed safety boundaries.
This example shows how a patient could receive a plain-language explanation and a clear handoff. It is not a live product, study result, or substitute for the study team.
Any deployment would be shaped with Materna’s clinical, research, privacy, and product teams. The examples here are a concept—not a claim of an existing integration.
Materna reviews the product, study, and safety information before it is used in patient-facing answers.
Define consent, privacy, retention, and permitted data flows with Materna before launch.
Choose one patient-support use case, an approved workflow, and clear criteria for evaluating it.