Last reviewed · How we verify
NCT02324062: HCP
Cancer Genetics Hereditary Cancer Panel Testing
trial testing Questionnaires in Hereditary Breast and Ovarian Cancer in 1,511 participants. Completed in 31 August 2020.
31 August 2020
Quick facts
| Lead sponsor | University of Southern California |
|---|---|
| Status | Completed |
| Study type | OBSERVATIONAL |
| Enrollment | 1,511 |
| Start date | 12 June 2014 |
| Primary completion | 31 August 2020 |
| Estimated completion | 31 August 2020 |
| Sites | 2 locations across United States |
Drugs / interventions tested
- Questionnaires
- Blood Draw and Baseline Questionnaire
Conditions studied
- Hereditary Breast and Ovarian Cancer — all drugs for Hereditary Breast and Ovarian Cancer →
Sponsor
University of Southern California
Who can join
Eligibility, any sex, with Hereditary Breast and Ovarian Cancer. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study is about understanding the use of a genetic test (Myriad Genetics myRisk panel) that analyzes 25 genes related to different hereditary cancer conditions. The investigators hope to learn more about how this type of genetic test is used clinically. The investigators also hope to understand more about the experience of individuals and families who undergoing this test of genetic testing.
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:
- PubMed search for NCT02324062
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other trials of Questionnaires
Trials testing the same drug.
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- NCT07344649 — Turkish Validation of the Nijmegen Questionnaire in COPD · recruiting
- NCT06836414 — Lung Cancer Screening CT for Firefighters · NA · withdrawn
Other recruiting trials for Hereditary Breast and Ovarian Cancer
Currently open trials in the same condition.
- NCT05130606 — CONTIGO - A Narrative Intervention to Enhance Genetic Counseling and Testing · NA · recruiting
- NCT03246841 — Investigation of Tumour Spectrum of Germline Mutations in Breast and Ovarian Cancer Genes. · NA · active not recruiting
- NCT03050268 — Familial Investigations of Childhood Cancer Predisposition · recruiting
- NCT03124212 — Cascade Genetic Testing for Hereditary Breast/Ovarian Cancer and Lynch Syndrome in Switzerland · recruiting
Other University of Southern California trials
Trials by the same sponsor.
- NCT07288463 — Hearing Loss and Genetic Risks for Alzheimer's Disease and Related Dementia · NA · not yet recruiting
- NCT05914233 — Non-invasive Ultrasound Retinal Stimulation for Vision Restoration · NA · not yet recruiting
- NCT06163664 — Role of ChatGPT in Vestibular Schwannoma Management · NA · withdrawn
- NCT07332312 — A Culturally Informed Patient Navigation Program (CFPN) to Reduce Delays Between Diagnosis and Treatment in American Ind · NA · not yet recruiting
- NCT07290478 — Encouraging Older Adults and Adults With Serious Illness to Designate a Health Care Proxy · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT02324062 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by University of Southern California
- Last refreshed: 18 February 2026
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/NCT02324062.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing