Clinical trial
Treatment of Endometrial Hyperplasia With an Intrauterine Device (IUD)
NCT00123175 · Milton S. Hershey Medical Center, Other · Withdrawn
Key facts
| NCT number | NCT00123175 |
|---|---|
| Title | Treatment of Endometrial Hyperplasia With an Intrauterine Device (IUD) |
| Official title | Levonorgestrel Containing Intrauterine Device in the Treatment of Endometrial Hyperplasia Without Atypia |
| Lead sponsor | Milton S. Hershey Medical Center, Other |
| Collaborators | Center for Research on Women and Newborn Health |
| Status | Withdrawn |
| Phase | Phase 1/Phase 2 |
| Study type | Interventional |
| Conditions | Endometrial Hyperplasia |
| Intervention type | Device |
| Interventions | Intrauterine Device |
| Enrollment | 0 |
| Start date | Sep 1, 2009 |
| Primary completion | Sep 1, 2011 |
| Completion | Sep 1, 2011 |
| First posted | Jul 22, 2005 |
| Last update posted | Jan 8, 2013 |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: