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Probiotic in treatment of pneumonia

The effect of probiotic on improvement of pneumonia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200107046047N1
Enrollment
100
Registered
2020-04-07
Start date
2018-01-30
Completion date
Unknown
Last updated
2020-05-18

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

Conditions

Bacterial pneumonia. Bacterial pneumonia, not elsewhere classified

Interventions

Intervention 1: Intervention group: Two sachets of probiotic daily for 5 days, product of Biology fermentation company. Intervention 2: Control group: Two sachets of placebo daily for 5 days, product

Sponsors

Kashan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 12 years. Bacterial pneumonia is early diagnosis. Taking written consent from the patient to participate in the study. The patient is able to eat probiotic or placebo. Pneumonia is not very severe requiring admission in ICU.

Exclusion criteria

Exclusion criteria: The patient has no previous heart failure and pulmonary edema. No underlying pulmonary disease. Intolerance or allergy to probiotic. Dissatisfaction of patients for participating in study.

Design outcomes

Primary

MeasureTime frame
Duration of hospitalization. Timepoint: From hospitalization to discharge. Method of measurement: Number of days of hospitalization based on patient file and questionnaire.;Dyspnea duration. Timepoint: From hospitalization to discharge. Method of measurement: Completion of questionnaire and examination of patient.;Tachypnea duration. Timepoint: From hospitalization to discharge. Method of measurement: Completion of questionnaire and examination of patient.;Duration of cough. Timepoint: From hospitalization to discharge. Method of measurement: Completion of questionnaire and examination of patient.;Duration of lung auscultation rales. Timepoint: From hospitalization to discharge. Method of measurement: Patient examination and questionnaire completion.;Duration of fever. Timepoint: From hospitalization to discharge. Method of measurement: Patient examination and questionnaire completion.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr ?Ahmad Najafi

Kashan University of Medical Sciences

a.najafi1975@yahoo.com+98 31 5533 0489

Outcome results

None listed

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