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NCT03119285 · ClinicalTrials.gov registry record

Genes Contributing to Hereditary Ovarian Cancer in Women and BRCA1/2 Wildtype Families

A clinical trial of Ovarian Cancer, sponsored by University of Washington.

Completed
Registry status
34
Enrollment target
1
Study location

NCT03119285 is a study of Ovarian Cancer that has completed, run by University of Washington. The registered enrollment target is 34 participants, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT03119285, a study of Ovarian Cancer, has completed, sponsored by University of Washington.

COMPLETED
Registry status
34 participants
Enrollment target
1
Study location

Study Summary

The investigators propose to test for non-BRCA1/2 mutations in new and existing families with hereditary ovarian cancer in order to better define penetrance and associated malignancies of rare ovarian cancer susceptibility genes. The hypothesis is at least one third of hereditary ovarian carcinoma families wildtype for BRCA1/2 can be solved using an updated version of BROCA (BROCA-HR) that targets 47 genes, including all known ovarian cancer genes and additional candidate genes in related pathways. The objective is to identify families with mutations in rare ovarian cancer susceptibility genes and test both affected and unaffected family members, thereby generating a rough estimate of penetrance for each mutated gene as well as identify new ovarian cancer susceptibility genes. The investigators also plan to enroll self identified African America women, who have been drastically under-represented in clinical cancer genetic testing programs and in OC susceptibility research.

Conditions Studied

Study Locations (1)

Washington

  • University of Washington - Seattle

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2013-04
Est. Completion 2022-01-31

Sponsor

University of Washington

1,048 total trials

What the Registry Record Tells You About NCT03119285

The ClinicalTrials.gov registry entry for NCT03119285 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 34 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 729-participant average among 322 other Ovarian Cancer trials with a reported enrollment target (95% lower). The listed sponsor is University of Washington, which has 1,048 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Ovarian Cancer appearing as the primary indexed condition, and to 0 interventions.

NCT03119285 reports 1 study location spanning 1 distinct geographic area - top geographies include Washington.

Frequently Asked Questions

What is clinical trial NCT03119285 about?

NCT03119285 is a clinical study titled "Genes Contributing to Hereditary Ovarian Cancer in Women and BRCA1/2 Wildtype Families". The investigators propose to test for non-BRCA1/2 mutations in new and existing families with hereditary ovarian cancer in order to better define penetrance and associated malignancies of rare ovarian cancer susceptibility genes. The hypothesis is at least one third of hereditary ovarian carcinoma f...

What is the current status of trial NCT03119285?

This trial is currently completed. The enrollment target is 34 participants. The study started on 2013-04. Estimated completion is 2022-01-31.

What conditions does trial NCT03119285 study?

This clinical trial studies the following conditions: Ovarian Cancer.

Who is sponsoring clinical trial NCT03119285?

This trial is sponsored by University of Washington, which has 1,048 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03119285 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.