Microbiome of Urologic Chronic Pelvic Pain Syndrome

Key facts

Sponsor

Johns Hopkins University

Principal Investigator

Arthur L Burnett, MD, FACS

Johns Hopkins University

Intervention

Genitourinary Specimen Collection(procedure)

Eligibility

18-70 years · All sexes

Timeline

2013 – 2015

Study locations (1)

• Johns Hopkins Hospital, Baltimore, Maryland, United States

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

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