Women's Health · Community · Clinical Research

Healing beyond limits, together.

LUMIKEI MED is where women get real answers, connect with clinicians and researchers, and access the clinical trials historically built without them in mind.

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Live on the platform

This week

"How long did it take you to get an endometriosis diagnosis?" — 34 women replied, including a research scientist.

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12,400+
Women in community
38
Audited trials listed
150+
Clinicians & researchers
92%
Participant satisfaction
What you get

One platform, four ways to be supported

Built for the everyday questions and the moments that need real clinical expertise.

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Community

Ask questions, share what worked, and get answers from other women — and from verified professionals and researchers.

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Education

Plain-language articles on women's health, plus a full breakdown of how clinical trials actually work.

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Trials & Support

Browse audited, inclusive trials matched to your health profile, and request the specific support you need to join.

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Workshops & Events

Live sessions with clinicians on cycles, menopause, mental health, heart health, and more.

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For women

Your health data, working for you — not against you.

Create a confidential health profile once. We use it only to match you with clinical trials you're actually eligible for, and to make sure any support you need — transportation, childcare, translation — is on the table before you commit to anything.

  • GDPR-aligned data handling, always under your control
  • No obligation — reviewing a match never enrolls you automatically
  • Backed by our real intake form, built with clinical research partners
Build your health profile
Path to a trial
1
Create your profile

A few minutes, fully confidential.

2
Get matched

Against audited, active trial criteria.

3
Review & request support

See what's offered before you say yes.

4
Talk to the trial's clinical team

You're always in control of next steps.

Clinical trials

Run trials that actually reflect the population you're treating.

We audit your protocol against inclusive-design and FDA diversity guidance, help you design around the gaps, then match you directly with consenting, eligible candidates from our member base.

Have a clinical trial? Sign up
Clinical trials

Subscribe, list your trial, get matched — and stay compliant.

List your trial with full requirements and eligibility criteria. Our team audits it to reduce your regulatory risk and improve inclusivity, then we match you to candidates from a database of women who've opted in.

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Pre-submission audit against FDA diversity guidance
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Inclusive trial design consulting
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Direct candidate matching
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Ongoing compliance support

Made for you, not the norm.

Because healing isn't one-size-fits-all — and neither is our platform.

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