Biology of Osteosarcoma (BOOST) Registry and Biobank

University of Minnesota (UMN)

Status: Completed

Conditions: Osteosarcoma

Study type: Observational

Funder types: Other

Identifiers

NCT03225872

2016NTLS073

Details and patient eligibility

About

Osteosarcoma is very rare cancer of the bone. The investigator started the BOOST registry and biobank to make sure every patient has the opportunity to participate in research.

Full description

Summary to include:

1. Samples of saliva, blood and/or other stored material such as slides or leftover diagnostic material. If available the investigator may ask you for deciduous (baby) teeth.
2. Questionnaire information, including health history, growth and development, physical activity and family medical history information.
3. If you have been diagnosed with a osteosarcoma or another condition the investigator is interested inthe investigator will ask you release medical record information relating to diagnosis and treatment of osteosarcoma, other cancers, blood disorders, and similar conditions. If this step applies to you then you will be asked to sign a separate form.
4. You may be asked to contact your biological parents and full biological siblings to ask them about participating in the study.
5. If you agree you may be contacted in the future. You will be able to decline any future information or studies at any point.

Enrollment: 362 patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Proband Inclusion criteria: A diagnosis or suspected diagnosis of osteosarcoma (ICCC 9180-9200)

Family member inclusion criteria: Biological parents and full biological siblings of a case diagnosed with osteosarcoma (ICCC 9180-9200)

Exclusion criteria

• Does not understand English.

Trial design

362 participants in 1 patient group

Osteosarcoma patients and family members

Description:

Osteosarcoma patients and family members