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Ultrasound and Biopsy for Endometrial Hyperplasia
N/A
Waitlist Available
Led By Richard Legro, M.D.
Research Sponsored by Milton S. Hershey Medical Center
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
* Postmenopausal obese subjects, who have diabetes or a prediabetic state, or hypertension
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up end of study
Awards & highlights
No Placebo-Only Group
Summary
The investigators hypothesize that endometrial thickness will be a significant predictor of endometrial hyperplasia in a postmenopausal female population with metabolic syndrome: diabetes and/or insulin resistance, hypertension, and obesity.
Eligible Conditions
- Endometrial Hyperplasia
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowTimeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ end of study
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~end of study
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Endometrial Hyperplasia
Secondary study objectives
Endometrial Cancer
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Ultrasound and BiopsyExperimental Treatment1 Intervention
Transvaginal Ultrasound and Endometrial Biopsy
Find a Location
Who is running the clinical trial?
Center for Research on Women and HealthUNKNOWN
Milton S. Hershey Medical CenterLead Sponsor
510 Previous Clinical Trials
2,796,413 Total Patients Enrolled
1 Trials studying Endometrial Hyperplasia
Richard Legro, M.D.Principal InvestigatorPenn State College of Medicine
5 Previous Clinical Trials
232 Total Patients Enrolled
1 Trials studying Endometrial Hyperplasia
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