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Recruiting NCT06909409

D Vitamin and Alveolar Macrophages in Idiopathic Pulmonal Fibrosis

Observational Idiopathic Pulmonary Fibrosis (IPF)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Idiopathic Pulmonary Fibrosis (IPF). Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Denmark
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The goal of this observational study is to gain deeper insights into human macrophages and vitamin D, and their interplay, within Idiopathic Pulmonary Fibrosis (IPF). The overall questions, it aims to answer, are the following: Do IPF patients suffer from systemic and local (pulmonary) insufficient levels of vitamin D? Do IPF patients suffer from pro-fibrotic and pro-inflammatory pulmonary macrophages?

Primary outcome measures

  • Vitamin D status [Time frame: At enrollment]
  • Pulmonary macrophages [Time frame: At enrollment]
Secondary outcome measures (1)
  • Biomarker levels in blood and BAL samples [Time frame: At enrollment]

Eligibility criteria

Inclusion criteria

  • A clinical diagnosis of IPF, non-IPF ILD or lung cancer
  • A signed informed consent

Exclusion criteria

  • Do not speak Danish/Do not understand Danish

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Denmark · 1 center
  • Aarhus University Hospital, Denmark — Aarhus N

Identifiers

NCT: NCT06909409 · 1-10-72-166-23

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗