CONDOR Prospective Clinical Database

Overview

About this study

The purpose of this study is to generate a clinical data source for the analysis of dural arteriovenous fistulas (dAVFs) pathophysiology, natural history, and clinical determinants of outcomes. Clinical data will be prospectively collected for consented patients.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria: 

  • Confirmed diagnosis of intracranial or spinal dural arteriovenous fistula

  • At least 18 years old

  • Willing to provide consent or have a LAR provide consent

  • Only in the patient subpopulation with tinnitus, surveys on quality of life patient reported outcomes will be recorded.

 Exclusion Criteria: 

  • No records available pertaining to intracranial or spinal dural Arteriovenous Fistula

Note: Other protocol defined Inclusion/Exclusion Criteria may apply. 

Eligibility last updated 11/03/2025. Questions regarding updates should be directed to the study team contact.

 

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Jacksonville, Fla.

Mayo Clinic principal investigator

W Fox, M.D.

Contact us for the latest status

More information

Publications

Publications are currently not available

Additional contact information

Non-cancer trials contact form

Phone: 800-664-4542 (toll-free)

International patient clinical studies questions