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The effect of probiotics in patients with obstructive pulmonary disease

The effect of probiotic on the clinical improvement of patients with chronic obstructive pulmonary disease (COPD)

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241226064174N1
Enrollment
40
Registered
2025-02-11
Start date
2025-03-08
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic obstructive pulmonary disease (COPD). Chronic obstructive pulmonary disease with (acute) exacerbation

Interventions

Intervention 1: Control group: placebo, A placebo capsule with the same appearance as the drug. Intervention 2: Intervention group: Treated with one Lactoker synbiotic capsule (Biot Khamtir Company, I

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: COPD patients with GOLD stage two to four, age over 50 years, and with a history of at least one COPD exacerbation leading to hospitalization during the last year

Exclusion criteria

Exclusion criteria: Patients with a history of previous pulmonary disease (other than COPD), acute coronary syndrome, CHF and hospitalization due to acute exacerbation of COPD in the last three weeks.

Design outcomes

Primary

MeasureTime frame
Changes in spirometric indices. Timepoint: Before, 6 months after the intervention. Method of measurement: Perform spirometry.

Secondary

MeasureTime frame
Dyspenea. Timepoint: Before and 6 months after the intervention. Method of measurement: MMRT,CAT index.;Quality of Life. Timepoint: Before and 6 months after the intervention. Method of measurement: questionnaire.;Severity of the disease. Timepoint: Before and 6 months after the intervention. Method of measurement: BODY index.;Number of exacerbations (outpatient and hospitalization). Timepoint: Before and 6 months after the intervention. Method of measurement: Question from the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmir Hossein Aref

Yazd University of Medical Sciences

amiraref73@gmail.com+98 35 3820 3419

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026