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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04019080
Other study ID # 180293
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 1, 2019
Est. completion date December 2021

Study information

Verified date July 2019
Source Karolinska University Hospital
Contact Carlson, RN
Phone +46737121597
Email lisa.carlson@sll.se
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The objective of the current research project is, by using high quality Swedish registry data, to evaluate use, tolerance and effect of anti-fibrotic drugs in IPF-patients. Secondary study objectives are to determine the clinical profile, determinants of treatment adherence, long-term safety and to describe the patient journey from the first sign of disease to end of treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 2021
Est. primary completion date December 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All subjects included in the Swedish IPF-registry

Exclusion Criteria:

- None

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Anti-fibrostic drugs
The real-Life use of anti-fibrotic drugs in patients with idiopathic pulmonary fibrosis in Sweden

Locations

Country Name City State
Sweden Karolinska University Hospital Stockholm

Sponsors (1)

Lead Sponsor Collaborator
Karolinska University Hospital

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Anti-fibrotic drugs among the patients recorded in the Swedish IPF-registry The use of anti-fibrostic drugs 2014-2020
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