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Study details
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Biological Effects of Quercetin in COPD Phase II

Temple University
NCT IDNCT06003270ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

30

Study length

about 1.7 years

Ages

40–80

Locations

1 site in PA

What this study is about

This trial is testing whether quercetin supplementation reduces inflammation and oxidative stress markers in people with chronic obstructive pulmonary disease (COPD). It involves a small number of participants receiving either a placebo, 1000 mg of quercetin daily, or 500 mg of quercetin daily for 638 days. The goal is to enroll approximately 30 participants.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take Placebo
  • 2.Take Quercetin 1000 mg
  • 3.Take Quercetin 500 MG

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Oral

How treatment is administered

Treatment Assignment
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

Immunological Agents

Drug routes

oral (Oral Tablet)

Endpoints

Primary: C-reactive protein (CRP), and surfactant protein (SP)-D in serum

Body systems

Respiratory