MyVHL: Patient Natural History Study

Purpose

MyVHL is a multi-patient database which helps researchers identify patterns across VHL patients. MyVHL provides you -and researchers -with more complete information about VHL, like how your lifestyle, medications, and other factors impact the disease and quality of life. These insights help you better understand the condition and help researchers know where to focus their efforts. Due to its rarity, there is less understanding of VHL and the factors that may have an impact. The data individuals provide in MyVHL helps researchers identify and uncover factors that may increase risk, inhibit or slow tumor growth, or lead to an effective cure.

Conditions

  • Von Hippel-Lindau Disease
  • Hereditary Leiomyomatosis and Renal Cell Cancer
  • Birt-Hogg-Dube Syndrome
  • SDHB Gene Mutation

Eligibility

Eligible Ages
All ages
Eligible Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • All patients with von Hippel-Lindau Disease (VHL)

Exclusion Criteria

Study Design

Phase
Study Type
Observational [Patient Registry]
Observational Model
Cohort
Time Perspective
Other

Recruiting Locations

VHL Alliance
Boston, Massachusetts 02132
Contact:
Joshua Mann, MPH
617-277-5667
josh.mann@vhl.org

More Details

Status
Recruiting
Sponsor
Joshua Mann, MPH

Study Contact

Joshua Mann, MPH
161727756674
josh.mann@vhl.org