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The effect of probiotics on blood parameters

Effects of probiotic supplementation on blood parameters and some anthropometric indicators in head trauma patients admitted to the ICU

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014060416221N2
Enrollment
60
Registered
2014-06-25
Start date
2013-03-21
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

Condition 1: Injuries to the head. Condition 2: Injuries to the head. Condition 3: Injuries to the head. Condition 4: Injuries to the head. Superficial injury of head Intracranial injury Other and unspecified injuries of head Fracture of skull and facial bones

Interventions

Intervention 1: Two probiotic supplements daily for two weeks of oral in the intervention group. Intervention 2: In the control group, no treatment. Before and two weeks after the study were evaluated
Treatment - Drugs
Two probiotic supplements daily for two weeks of oral in the intervention group
In the control group, no treatment. Before and two weeks after the study were evaluated anthropometric indices and blood parameters.

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 49 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with head injur? age between 49-15 years Exclusion criteria: gastric intolerance; GCS = 3-5; transfusion of blood and its products

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Blood parameters. Timepoint: Before Intervention and two weeks after the intervention. Method of measurement: milligrams per deciliter, using laboratory apparatus.;Anthropometric indicators. Timepoint: Before Intervention and two weeks after the intervention. Method of measurement: Centimeter, usiing meter.

Secondary

MeasureTime frame
Gastrointestinal digestion. Timepoint: Before and during the intervention. Method of measurement: Questionnaire in terms of defecation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Tajabadi

Sabzevar University of Medical Sciences

alitaj58@yahoo.com+98 57 1444 6070

Outcome results

None listed

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