Skip to content
Study details
Enrolling now

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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take Placebo
  • 2.Take Quercetin 1000 mg
  • 3.Take Quercetin 500 MG
PhasePhase 2
DrugQuercetin 1000 mg
Routeoral
Primary goalC-reactive protein (CRP), and surfactant protein (SP)-D in serum

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low12%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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