Practice Patterns Among Gynecologic Oncologists on Tumor Genetic Testing in Endometrial Cancer
NCT ID: NCT05877404
Last Updated: 2024-04-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
112 participants
OBSERVATIONAL
2023-08-15
2024-02-28
Brief Summary
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Detailed Description
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Secondary Objectives:
* Explore the use of informed consent in tumor genetic testing in endometrial cancer
* Explore clinician confidence in utilizing tumor genetic testing to guide treatment decisions.
* Explore the impact of recent publications regarding immunotherapy on the use of tumor genetic testing in endometrial cancer.
Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Gynecologic Oncologists
Gynecologic Oncologists and gynecologic oncology fellows-in-training from around the world, who are members of the Society of Gynecologic Oncology (SGO).
Surveys
Survey on practice patterns surrounding tumor genetic testing in endometrial cancer.
Interventions
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Surveys
Survey on practice patterns surrounding tumor genetic testing in endometrial cancer.
Eligibility Criteria
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Inclusion Criteria
* Gynecologic Oncologist or Gynecologic Oncology Fellow-in-Training
ALL
Yes
Sponsors
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National Cancer Institute (NCI)
NIH
Wake Forest University Health Sciences
OTHER
Responsible Party
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Principal Investigators
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Kathryn Weaver, PhD, MPH
Role: PRINCIPAL_INVESTIGATOR
Wake Forest Baptist Comprehensive Cancer Center
Locations
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Wake Forest Baptist Comprehensive Cancer Center
Winston-Salem, North Carolina, United States
Countries
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Other Identifiers
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WFBCCC 99323
Identifier Type: OTHER
Identifier Source: secondary_id
NCI-2023-05554
Identifier Type: OTHER
Identifier Source: secondary_id
IRB00097221
Identifier Type: -
Identifier Source: org_study_id
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