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Investigating Significant Health Trends in Idiopathic Pulmonary Fibrosis

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01695408
Acronym
INSIGHTS-IPF
Enrollment
1232
Registered
2012-09-28
Start date
2012-10-31
Completion date
2021-12-31
Last updated
2022-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Idiopathic Pulmonary Fibrosis

Keywords

Drug Treatment, Treatment pathways, Clinical routine, Registry, Outcomes, Survival, Patient-related outcomes, Quality of life, Steroids, Azathioprine, N-Acetylcysteine, Pirfenidone, Tyrosine kinase inhibitors, Nintedanib, multicenter, Germany, Safety, Adverse event

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.

Interventions

None listed

Sponsors

GWT-TUD GmbH
CollaboratorOTHER
Boehringer Ingelheim
CollaboratorINDUSTRY
Technische Universität Dresden
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

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

* None

Design outcomes

Primary

MeasureTime frame
Clinical course of IPF (in terms of symptoms, lung function, survival)up to 5 years after inclusion

Secondary

MeasureTime frameDescription
Characteristics of patients with IPFup to 5 years after inclusion
Treatment pathwaysup to 5 years after inclusion
Functionality and quality of lifeup to 5 years after inclusionSt. Georges Respiratory Questionnaire; University of California Shortness of Breath Questionnaire; EuroQuol 5 dimensions

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 21, 2026