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NCT06926816 · ClinicalTrials.gov registry record · NA

Universal Genetic Testing for Cancer Risk Reduction

A NA study of Genetic Testing, sponsored by NYU Langone Health.

Recruiting
Registry status
NA
Development phase
600
Enrollment target
1
Study location

NCT06926816: Recruiting NA study of Genetic Testing, sponsored by NYU Langone Health.

NCT06926816 is a NA study of Genetic Testing that is actively recruiting participants, run by NYU Langone Health. The registered enrollment target is 600 participants, roughly in line with the 561-participant average among 7 other Genetic Testing trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06926816, a NA study of Genetic Testing, is actively recruiting participants, sponsored by NYU Langone Health.

RECRUITING
Registry status
NA
Development phase
600 participants
Enrollment target
1
Study location

Study Summary

The purpose of this research study is to see if offering genetic testing for cancer-related genes is feasible and acceptable for patients presenting for gynecology clinic visits, instead of needing to see specialized providers or needing to meet specific criteria. The primary aim to assess the proportion of patients who undergo genetic testing, and the proportion of patients with pathogenic variants.

Primary Outcome

Outcome measure will be assessed via review of electronic medical record (EMR).

Conditions Studied

Interventions

  • GENETIC Natera® Empower™ hereditary cancer panel test
  • OTHER Specialist Referral

Study Locations (1)

New York

  • NYU Langone Health - New York

Trial Details

FieldValue
Enrollment Target 600 participants
Start Date 2025-03-04
Est. Completion 2027-12-31
Phase NA
NYU Langone Health

1,164 total trials

What NCT06926816 shows while recruiting

NCT06926816 is an interventional study that assigns participants to a tested intervention. The registered 600 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 561-participant average among 7 other Genetic Testing trials with a reported enrollment target.

The record links to 1 condition, with Genetic Testing appearing as the primary indexed condition, and to 2 interventions - of which Natera® Empower™ hereditary cancer panel test is the first listed.

NCT06926816 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT06926816 about?

NCT06926816 is a clinical study titled "Universal Genetic Testing for Cancer Risk Reduction". The purpose of this research study is to see if offering genetic testing for cancer-related genes is feasible and acceptable for patients presenting for gynecology clinic visits, instead of needing to see specialized providers or needing to meet specific criteria. The primary aim to assess the propo...

What is the current status of trial NCT06926816?

This trial is currently recruiting. It is a NA study. The enrollment target is 600 participants. The study started on 2025-03-04. Estimated completion is 2027-12-31.

What conditions does trial NCT06926816 study?

This clinical trial studies the following conditions: Genetic Testing.

What interventions are being tested in trial NCT06926816?

The interventions under investigation include: Natera® Empower™ hereditary cancer panel test (GENETIC), Specialist Referral (OTHER).

Who is sponsoring clinical trial NCT06926816?

This trial is sponsored by NYU Langone Health, which has 1,164 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06926816 being conducted?

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

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT06926816, the US trial registry maintained by the National Library of Medicine. NCT06926816 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.