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NCT03421327

Genetic Risk: Whether, When, and How to Tell Adolescents

Completed Last updated 7 February 2019
What this trial tests

trial in Huntington Disease in 85 participants. Completed in 31 December 2018.

Timeline
1 September 2017
Primary endpoint
31 December 2018
31 December 2018

Quick facts

Lead sponsorJohns Hopkins University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment85
Start date1 September 2017
Primary completion31 December 2018
Estimated completion31 December 2018
Sites1 location across United States

Conditions studied

Sponsor

Johns Hopkins University

Who can join

15 and older, any sex, with Huntington Disease or Hereditary Breast and Ovarian Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study is being conducted to learn more about family communication of genetic risk information. Semi-structured interviews lasting up to one hour will be conducted with three populations: parent/child pairs at risk for Huntington's Disease, parent/child pairs at risk for hereditary cancer, and genetic counselors.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Huntington Disease

Currently open trials in the same condition.

Other Johns Hopkins University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03421327.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing