Interstitial Lung Disease Clinical Trials

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Study on the Efficacy of Quercetin Intake in Patients With Idiopathic Pulmonary Fibrosis and Non-Idiopathic Pulmonary Fibrosis. A Two-arm, Prospective Randomized Controlled Clinical Trial.

Status: Recruiting
Location: See location...
Intervention Type: Dietary supplement, Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Fibrotic interstitial lung diseases (F-ILDs), including both idiopathic pulmonary fibrosis (IPF) and non-IPF, are chronic and progressive lung diseases characterized by excessive scarring of lung tissue, leading to declining lung function, respiratory failure, and high mortality, despite the currently approved antifibrotic treatment. While its exact cause remains unknown, pulmonary fibrosis is strongly linked to aging, genetic predisposition, environmental factors, and cellular senescence. Ongoing research aims to identify reliable biomarkers and develop targeted treatments to enhance patient outcomes. This randomized controlled trial will examine the effects of quercetin supplementation (500 mg/day for two 12-week cycles, with one 8-week washout periods) on telomere length, senescence-associated secretory phenotype (SASP) factors, and lung function in patients with IPF and F-ILDs. A total of 100 patients will be recruited, with half receiving quercetin (despite their standard of care therapy) and the other half receiving standard care (SOC). Primary outcomes will include changes in telomere length, SASP protein levels (IL-6, MMPs), fractional exhaled nitric oxide (FeNO), spirometry (FVC decline), and oscillometry measurements. Additionally, quality of life will be assessed using the L-IPF Questionnaire. This study aims to explore quercetin's potential to reduce fibrosis, decrease inflammation, and improve lung function in F-ILDs, offering new insights into potential novel strategies for F-ILD management.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients with an established diagnosis of IPF and Fibrotic ILD and will be eligible to participate in the study.

• The use of the approved standard of care antifibrotic therapy, either nintedanib or pirfenidone, and immunosuppressive therapy will be allowed as standard of care.

Locations
Other Locations
Greece
Respiratory Department, University Hospital of Heraklion, School of Medicine, University of Crete
RECRUITING
Heraklion
Contact Information
Primary
Ioanna Argyriou, MSc
ioannaar07@gmail.com
+302810371966
Backup
Eirini Vasarmidi, MD MSc PhD, Ass. Professor
Time Frame
Start Date: 2026-01-26
Estimated Completion Date: 2029-01-31
Participants
Target number of participants: 100
Treatments
Active_comparator: Standard of care (SOC) treatment
Standard of care based on the specific ILD
Experimental: Quercetin (dietary supplement)
Sponsors
Leads: Katerina M. Antoniou

This content was sourced from clinicaltrials.gov