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Trials / Completed

CompletedNCT03115619

Quality of Life Study in Participants With IPF Under Pirfenidone Treatment

A Multicenter, Post-Marketing, Non-Interventional, Observational Study to Evaluate Quality of Life in Patients in Greece With Idiopathic Pulmonary Fibrosis Under Treatment With Pirfenidone - The Pneumon Study

Status
Completed
Phase
Study type
Observational
Enrollment
102 (actual)
Sponsor
Hoffmann-La Roche · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This multicenter, post-marketing, observational study will evaluate quality of life in participants with Idiopathic Pulmonary Fibrosis (IPF) under treatment with pirfenidone (Esbriet).

Conditions

Interventions

TypeNameDescription
DRUGPirfenidoneParticipants will receive pirfenidone therapy as per clinical practice or summary of product characteristics (SmPC).

Timeline

Start date
2017-04-18
Primary completion
2020-01-10
Completion
2020-01-10
First posted
2017-04-14
Last updated
2020-08-21

Locations

7 sites across 1 country: Greece

Regulatory

Source: ClinicalTrials.gov record NCT03115619. Inclusion in this directory is not an endorsement.

Quality of Life Study in Participants With IPF Under Pirfenidone Treatment (NCT03115619) · Clinical Trials Directory