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Clinical Trials/NCT01695408
NCT01695408
Completed
Not Applicable

Investigating Significant Health Trends in IPF (INSIGHTS-IPF). Nationwide Prospective Registry.

Technische Universität Dresden5 sites in 1 country1,232 target enrollmentOctober 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Idiopathic Pulmonary Fibrosis
Sponsor
Technische Universität Dresden
Enrollment
1232
Locations
5
Primary Endpoint
Clinical course of IPF (in terms of symptoms, lung function, survival)
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Idiopathic pulmonary fibrosis (IPF), a manifestation of chronic progressive fibrosing interstitial pneumonia,ia a rare disease. Current treatment options are limited, and the mean survival time of the newly diagnosed (mostly elderly) patients is only about 2-3 years. As in Europe data are limited on the characteristics and management of such patients, INSIGHTS-IPF was initiated as a new registry that documents newly diagnosed (incident) and prevalent patients with confirmed IPF diagnosis prospectively.The registry will contribute to the optimization of the management of IPF patients in the long term.

Detailed Description

INSIGHTS-IPF will report current and comprehensive data on Idiopathic Pulmonary Fibrosis (IPF) in the long-term. Baseline (cross-sectional part): Description of characteristics of IPF patients in terms of * key (socio-) demographic data * IPF risk factors, comorbidities * methods used for IPF diagnosis * IPF disease severity and manifestation (including lung function, cardiopulmonary exercise testing and/or exercise capacity if available, laboratory values, biomarkers) * IPF treatment (detailed information on prescribed drugs and doses; non-pharmacological treatment; listing and score for lung transplantation) * assessment of patient-related outcomes (PRO) such as quality of life Follow-up (prospectively up to at least 2 years after inclusion): * Clinical course of IPF (e.g. in terms of symptoms, lung function, exercise capacity if available) * Documentation of treatment pathways (switch/add-on/discontinuation of medication), and of non-pharmacological treatment (e.g. start of long term oxygen therapy; new listing for lung transplantation)Outcomes/events (such as acute respiratory worsening, exacerbations, hospitalisation due to any cause and due to IPF, other complications, survival) * Patient-related outcomes such as quality of life, assessed once a year(for comparison with baseline) * Resource use for pharmacoeconomic analyses.

Registry
clinicaltrials.gov
Start Date
October 2012
End Date
December 31, 2021
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • At least 18 years of age
  • Written informed consent for participation in the registry
  • Newly diagnosed (incident) or known (prevalent) IPF (based on diagnosis of treating physician)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Clinical course of IPF (in terms of symptoms, lung function, survival)

Time Frame: up to 5 years after inclusion

Secondary Outcomes

  • Treatment pathways(up to 5 years after inclusion)
  • Characteristics of patients with IPF(up to 5 years after inclusion)
  • Functionality and quality of life(up to 5 years after inclusion)

Study Sites (5)

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