ClinicalTrials.Veeva

Menu

Treatment of Endometrial Hyperplasia With an Intrauterine Device (IUD)

Penn State Health logo

Penn State Health

Status and phase

Withdrawn
Phase 2
Phase 1

Conditions

Endometrial Hyperplasia

Treatments

Device: Intrauterine Device

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this research is to determine the effectiveness of the intrauterine device (IUD) called Mirena when compared to the Provera tablets used in treating this condition.

Full description

Endometrial hyperplasia without atypia is a condition usually caused by excessive stimulation of the uterine lining (endometrium) by estrogens, and may cause irregular bleeding as a presenting symptom, but rarely may progress to endometrial cancer, which makes treatment important. The only treatment approved so far is medroxyprogesterone acetate tablets (progesterone), also known as Provera.

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Histologic diagnosis of simple or complex endometrial hyperplasia without atypia
  • Normal pap smear within one year

Exclusion criteria

  • Diabetes
  • Family history of endometrial cancer
  • Contraindications for the intrauterine device

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems