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Enrolling by invitation NCT05314426

Mayo Clinic Phage Program Biobank

Observational Bacteriophage Therapy

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Bacteriophage Therapy. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of this study is to help scientists and clinicians discover answers to research questions related to antibiotic-resistant bacterial infections, and the role that phage therapy plays as a possible treatment.

Primary outcome measures

  • Enrollment of study participants [Time frame: 5 years]
  • Collection of biospecimens [Time frame: 5 years]
  • Medical record review [Time frame: 5 years]
  • Increase treatment options and level of care for patients with bacterial infections [Time frame: 5 years]

Eligibility criteria

Inclusion criteria

  • ≥ 18 years of age.
  • Able to provide informed consent.
  • Individual must have a future treatment plan to receive or has historically received phage therapy.

Exclusion criteria

  • Individuals , 18 years of age.
  • Unwilling/unable to provide informed consent.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Mayo Clinic Rochester — Rochester

Identifiers

NCT: NCT05314426 · 21-013112

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗