Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
70

Summary

Conditions
Cystic Fibrosis
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 18 years and 89 years
Gender
Both males and females

Description

To determine if elexacfator-tezacaftor-ivacaftor improves the signs and symptoms of CF-related sinus disease, before and after initiation of triple combination therapy, each subject will undergo sinus CT scan and complete questionnaires related to signs and symptoms of sinus disease.

To determine if elexacfator-tezacaftor-ivacaftor improves the signs and symptoms of CF-related sinus disease, before and after initiation of triple combination therapy, each subject will undergo sinus CT scan and complete questionnaires related to signs and symptoms of sinus disease.

Tracking Information

NCT #
NCT04056702
Collaborators
Cystic Fibrosis Foundation
Investigators
Principal Investigator: Jennifer TaylorCousar, M.D. National Jewish Health