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Identification of Genetic changes and other factors in hereditary breast and ovarian cancer

Identification of genetic and non-genetic confounding factors in hereditary breast and ovarian cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2020/02/023574
Enrollment
169
Registered
2020-02-25
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C50- Malignant neoplasm of breast Health Condition 2: C569- Malignant neoplasm of unspecifiedovary

Interventions

None listed

Sponsors

Dr T M A Pai Fellowship
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Known mutation in cancer susceptibility gene within the family Any patient with male breast cancer Personal history of breast cancer with one or more of following Early age of onset If diagnosed at Diagnosed at any age with: One or more close blood relative with breast cancer diagnosed at Two or more close blood relative with breast cancer at any age One or more close blood relative with invasive ovarian cancer Close male blood relative breast cancer.

Exclusion criteria

Exclusion criteria: Cancer individual without a family history Early death due to cancer or non-cancerous conditions Any psychological or genetic disorder with mental retardation Adoption and limited family size Patient not willing for genetic testing genetic counseling

Design outcomes

Primary

MeasureTime frame
ï?? To identify the frequency types and genetic variants of germline mutations among the patient presenting with high risk of hereditary cancer by NGS Cancer risk assessment based on the genetic and non-genetic factors in patient and at-risk family memberTimepoint: 3years

Secondary

MeasureTime frame
Presence of other non-genetic confounding factors and comparison between incidence of nongenetic factor among the patient with average and high risk and To develop a genetic variation database for public health purposeTimepoint: 3years

Countries

India

Contacts

Public ContactDr Karthik S Udupa

Manipal Academy of Higher Education

udupa.karthik@manipal.edu9845317153

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026