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NCT07382583 · ClinicalTrials.gov registry record
Development of a Shared Decision Tool to Facilitate Uptake of the Levonorgestrel-releasing Intrauterine System for the Primary Prevention of Endometrial Cancer
A clinical trial of Endometrial Cancer and Prevention, sponsored by M.D. Anderson Cancer Center.
- Recruiting
- Registry status
- 270
- Enrollment target
- 2
- Study locations
NCT07382583 is a study of Endometrial Cancer and Prevention that is actively recruiting participants, run by M.D. Anderson Cancer Center. The registered enrollment target is 270 participants, below the 523-participant average among 181 other Endometrial Cancer trials with a reported enrollment target (48% lower). The trial reports 2 study locations across 1 state.
The verdict
NCT07382583, a study of Endometrial Cancer and Prevention, is actively recruiting participants, sponsored by M.D. Anderson Cancer Center.
- RECRUITING
- Registry status
- 270 participants
- Enrollment target
- 2
- Study locations
Study Summary
To develop an educational tool to help patients and healthcare professionals make informed decisions about endometrial cancer and available prevention options for it (such as the use of a levonorgestrel-releasing intrauterine system \[LNG-IUS\]).
Conditions Studied
Interventions
- OTHER Survey using a questionnaire
Study Locations (2)
Texas
- The Harris Health System (LBJ) - Houston
- MD Anderson Cancer Center - Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 270 participants |
| Start Date | 2026-02-12 |
| Est. Completion | 2030-02-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07382583
The ClinicalTrials.gov registry entry for NCT07382583 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 270 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 523-participant average among 181 other Endometrial Cancer trials with a reported enrollment target (48% lower). The listed sponsor is M.D. Anderson Cancer Center, which has 2,692 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Endometrial Cancer appearing as the primary indexed condition, and to 1 intervention - of which Survey using a questionnaire is the first listed.
NCT07382583 reports 2 study locations spanning 1 distinct geographic area - top geographies include Texas.
Frequently Asked Questions
What is clinical trial NCT07382583 about?
NCT07382583 is a clinical study titled "Development of a Shared Decision Tool to Facilitate Uptake of the Levonorgestrel-releasing Intrauterine System for the Primary Prevention of Endometrial Cancer". To develop an educational tool to help patients and healthcare professionals make informed decisions about endometrial cancer and available prevention options for it (such as the use of a levonorgestrel-releasing intrauterine system \[LNG-IUS\]).
What is the current status of trial NCT07382583?
This trial is currently recruiting. The enrollment target is 270 participants. The study started on 2026-02-12. Estimated completion is 2030-02-01.
What conditions does trial NCT07382583 study?
This clinical trial studies the following conditions: Endometrial Cancer, Prevention, Levonorgestrel, Intrauterine Systems.
What interventions are being tested in trial NCT07382583?
The interventions under investigation include: Survey using a questionnaire (OTHER).
Who is sponsoring clinical trial NCT07382583?
This trial is sponsored by M.D. Anderson Cancer Center, which has 2,692 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07382583 being conducted?
This trial has 2 study locations across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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