Find trials
Search tips

Assessing the Portability of EHR Risk Prediction Models for Incident Symptomatic Fibroids

Overview

About this study

The purpose of this exploratory study is to develop, train and test an EHR risk prediction model for incident symptomatic fibroids. 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Women aged 18-60 without a prior history of fibroids.

Exclusion Criteria:

  • < 18 years of age. 

Note: Other protocol defined Inclusion/Exclusion criteria may apply.

Eligibility last updated 1/25/24. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Shannon Laughlin-Tommaso, M.D.

Contact us for the latest status

Contact information:

Shannon Laughlin-Tommaso M.D.

(507) 266-8700

LaughlinTommaso.Shannon@mayo.edu

Jacksonville, Fla.

Mayo Clinic principal investigator

Shannon Laughlin-Tommaso, M.D.

Contact us for the latest status

Contact information:

Megan Allyse Ph.D.

(904) 953-0368

Allyse.Megan@mayo.edu

More information

Publications

Publications are currently not available

More about research at Mayo Clinic

.
CLS-20570321

Mayo Clinic Footer