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OASIS-IPF (Idiopathic Pulmonary Fibrosis) Study

Boehringer Ingelheim logo

Boehringer Ingelheim

Status

Completed

Conditions

Idiopathic Pulmonary Fibrosis

Study type

Observational

Funder types

Industry

Identifiers

NCT03386994
1199-0296

Details and patient eligibility

About

Descriptive prospective non-interventional multicenter study based on newly collected data of Idiopathic Pulmonary Fibrosis patients followed-up for one year in secondary care settings (Pulmonology Services)

Enrollment

204 patients

Sex

All

Ages

40+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female and male patients ≥ 40 years of age
  • Patients diagnosed with Idiopathic Pulmonary Fibrosis (IPF) according to last ATS/ERS/JRS/ALAT IPF guideline for diagnosis and management consensus
  • Written informed consent prior to participation

Exclusion criteria

  • Inability for the patient to understand or complete the written Inform Consent or patients questionnaires or to understand Spanish
  • Current participation in any clinical trial
  • Patients for whom further follow-up is not possible at the enrolling site

Trial design

204 participants in 1 patient group

Idiopathic Pulmonary Fibrosis patients
Description:
all IPF patients

Trial documents
2

Trial contacts and locations

31

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Data sourced from clinicaltrials.gov

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