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NCT07743996Completed

Emotional and Social Experiences of Antifibrotic (AF) Therapy Among Idiopathic Pulmonary Fibrosis (IPF)/Progressive Pulmonary Fibrosis (PPF) Patients: A Real-World Study

A Real-World Study of the Perceived Emotional and Social Experiences Related to Antifibrotic Therapy in Patients With IPF and PPF: A Cross-Sectional Web-Based Survey

Source: ClinicalTrials.gov · Last updated 13 Oct 2026

Brief summary (registry, in English)

This is a cross-sectional study that will be conducted across Japan using an online patient-reported outcome questionnaire. This study tries to find out the attitudes toward and experiences of the emotional and/or social impact of side effects associated with antifibrotic (AF) treatment among Japanese patients with Idiopathic Pulmonary Fibrosis (IPF)/Progressive Pulmonary Fibrosis (PPF), and how are these attitudes associated with patients' individual characteristics.

Status (registry)
Completed
Study type
Observational
Enrollment
122 (actual)
First submitted
24 Jul 2026
Start date
1 Aug 2026
Primary completion date
30 Sept 2026
Lead sponsor
Boehringer Ingelheim
NCT number
NCT07743996

What you commit to

  • Study type: Observational
  • Participants enrolled: 122
  • From 1 Aug 2026 to the primary completion date, 30 Sept 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Patients treated with nerandomilast (including clinical trials)
  • Patients with PPF treated with pirfenidone

Other illness

  • Patients with malignant tumors

Other

  • Patients currently hospitalized

Who the study is looking for

  • Patients with IPF aged 40 years or older who received nintedanib or pirfenidone within the previous 4 weeks, or patients with PPF aged 18 years or older who received nintedanib within the previous 4 weeks
  • Patients capable of responding to a self-administered questionnaire

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Nippon Boehringer Ingelheim Co., Ltd.
Coordinator of this site? Confirm its status
TokyoJapanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.