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NCT04015102 · ClinicalTrials.gov registry record

A Registry for Hereditary Cancer Risk Assessment and Genetic Testing

A clinical trial, sponsored by Myriad Genetic Laboratories.

Completed
Registry status
255
Enrollment target

NCT04015102: Completed study, sponsored by Myriad Genetic Laboratories.

NCT04015102 is a clinical trial that has completed, run by Myriad Genetic Laboratories. The registered enrollment target is 255 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04015102 has completed, sponsored by Myriad Genetic Laboratories.

COMPLETED
Registry status
255 participants
Enrollment target

Study Summary

This prospective registry will evaluate the feasibility and impact of implementing standard cancer family history review and guideline-aligned genetic testing for men diagnosed with Prostate Cancer in community urology practices nationwide.

Primary Outcome

To see how practical it would be to integrate a standard hereditary cancer risk assessment , patient counseling and genetic testing process into the community urology practice setting. Also to evaluate the impact of the integrated process on provider and patient satisfaction. This registry will gather information to evaluate the feasibility of HCRA and genetic testing process integration in the Urology community practice setting. Analysis of the registry will compare historical pre-process integ

Trial Details

FieldValue
Enrollment Target 255 participants
Start Date 2019-03-06
Est. Completion 2020-10-30
Myriad Genetic Laboratories

15 total trials

What the finished NCT04015102 record still lists

NCT04015102 is an observational study that tracks outcomes without assigning an intervention. The registered 255 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 0 interventions.

NCT04015102 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04015102 about?

NCT04015102 is a clinical study titled "A Registry for Hereditary Cancer Risk Assessment and Genetic Testing". This prospective registry will evaluate the feasibility and impact of implementing standard cancer family history review and guideline-aligned genetic testing for men diagnosed with Prostate Cancer in community urology practices nationwide.

What is the current status of trial NCT04015102?

This trial is currently completed. The enrollment target is 255 participants. The study started on 2019-03-06. Estimated completion is 2020-10-30.

Who is sponsoring clinical trial NCT04015102?

This trial is sponsored by Myriad Genetic Laboratories, which has 15 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT04015102, the US trial registry maintained by the National Library of Medicine. NCT04015102 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.