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Effect of lactocare on pneumonia in critically ill patients

Effect of probiotic preparation, lactocare, on incidence of ventilator associated pneumonia in critically ill patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201411182582N10
Enrollment
80
Registered
2014-12-22
Start date
2015-03-20
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

pneumonia. Bacterial pneumonia, unspecified

Interventions

Intervention 1: All patients in control group will receive enteral capsules of placebo (1 capsule/12h) for one week in addition to standard VAP treatment. Intervention 2: All patients in intervention
Placebo
Treatment - Drugs
All patients in control group will receive enteral capsules of placebo (1 capsule/12h) for one week in addition to standard VAP treatment.
All patients in intervention group will receive enteral capsules of Lactocare (1 capsule/12h) for one week in addition to standard VAP treatment.

Sponsors

Research deputy of Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Inclusion: patients aging more than 18 years old and needing mechanical ventilation for a period of more than 48 hours Exclusion: History of pneumonia; dissatisfaction

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Ventilator Associated Pneumonia. Timepoint: 7 days. Method of measurement: Assay with Clinically infectious pulmonary score and bronchoscopy.

Secondary

MeasureTime frame
ICU length of stay. Timepoint: during ICU stay. Method of measurement: days that patient is stayed in ICU.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAta Mahmoodpoor

Anesthesiology department, Tabriz University of Medical Sciences

mahmoodpoora@tbzmed.ac.ir+98 41 3332 8009

Outcome results

None listed

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