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BREATHE Long-Term Follow-Up Study

E

Entellus Medical

Status

Completed

Conditions

Chronic Sinus Disease

Treatments

Device: FinESS Sinus Treatment

Study type

Observational

Funder types

Industry

Identifiers

NCT01319305
1743-001

Details and patient eligibility

About

This is a long-term follow-up of patients that participated in the BREATHE I study.

Enrollment

70 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Participated in BREATHE I study
  • Willing to sign consent and participate in long-term follow-up study

Exclusion criteria

  • None

Trial design

70 participants in 1 patient group

BREATHE I participatants
Treatment:
Device: FinESS Sinus Treatment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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