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NCT06485635Completed

Real-life-persistence to Antifibrotic Treatments

Source: ClinicalTrials.gov · Last updated 15 Apr 2026

Brief summary (registry, in English)

This study will help to better understand the persistence rate to antifibrotic (AF) treatment in real life in France and to identify potential areas for improvement by investigating the factors associated with a non-persistence rate to AF treatment. Primary objective of the study is to measure the percentage of patients still treated up to 30 months after AF treatment initiation.

Status (registry)
Completed
Study type
Observational
Enrollment
10646 (actual)
First submitted
10 Jun 2024
Start date
16 Oct 2024
Primary completion date
7 Apr 2026
Lead sponsor
Boehringer Ingelheim
NCT number
NCT06485635

What you commit to

  • Study type: Observational
  • Participants enrolled: 10646
  • From 16 Oct 2024 to the primary completion date, 7 Apr 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.

Other

  • No exclusion criteria will be applied.

Who the study is looking for

  • All patients with a reimbursement of AF treatment between 2018 and 2022 will be included for analysis.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Clinityx
Coordinator of this site? Confirm its status
Boulogne-BillancourtFranceUnknown status

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