ClinicalTrials.Veeva

Menu

Efficacy and Safety of Beta-glucan Supplement in Chronic Obstructive Pulmonary Disease Patients

C

Chulalongkorn University

Status

Not yet enrolling

Conditions

Chronic Obstructive Pulmonary Disease Patients

Treatments

Dietary Supplement: Beta-glucan supplement group
Dietary Supplement: Placebo group

Study type

Interventional

Funder types

Other

Identifiers

NCT05878834
Oh87/65

Details and patient eligibility

About

The objectives of this study are to evaluate Efficacy and safety of beta-glucan supplement in chronic obstructive pulmonary disease patients.

Full description

There are 72 patients in this study. They are randomly divided into 2 groups which are beta-glucan supplement group and placebo group. The supplement will be taken 1 capsule/day for 12 weeks. Forced expiratory volume in 1 second/Forced vital capacity, Modified Medical Research Council Dyspnea Score, Breathlessness, Cough, and Sputum Scale, 6 Minute Walk Test, Diffusing capacity for carbon monoxide, Tumor necrosis factor alpha, Interleukin-6, C-reactive protein, glutathione, aspartate transaminase, alanine transaminase, alkaline phosphatase, creatinine, and blood urea nitrogen are assessed before and after taking supplement 6 and 12 weeks.

Enrollment

72 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age more than 18 years
  • Chronic Obstructive Pulmonary Disease with Forced expiratory volume in 1 second/Forced vital capacity after receiving bronchodilator medicine more than 70%
  • No exacerbation and uncontrolled disease
  • 10 pack-years smoking history 10 pack-years but stop smoking more than 1 years
  • Willing to participate in this study

Exclusion criteria

  • Respiratory infection in 4 weeks
  • Lung cancer
  • Liver disease or kidney disease
  • Lung surgery history
  • Take kung supplement in 2 weeks
  • Take warfarin, clopidogrel, aspirin, or digoxin
  • Allergic to beta-glucan, broccoli, or quercetin
  • Cannot use Spirometry
  • Pregnancy and lactation

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

72 participants in 2 patient groups, including a placebo group

Beta-glucan supplement group
Experimental group
Description:
Beta-glucan supplement capsule composes of beta-glucan 250 mg, broccoli 75 mg, quercetin 50 mg.
Treatment:
Dietary Supplement: Beta-glucan supplement group
Placebo group
Placebo Comparator group
Description:
Placebo capsule is empty capsule.
Treatment:
Dietary Supplement: Placebo group

Trial contacts and locations

0

Loading...

Central trial contact

Pornanong Aramwit, Professor

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems