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Investigating the effect of synbiotics in professional futsal athletes

The effect of symbiotic supplementation on biochemical indicators of muscle damage, inflammation and nutritional status in professional futsal athletes

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100123003140N23
Enrollment
30
Registered
2024-03-21
Start date
2024-02-26
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Muscle damage.

Interventions

Intervention 1: Intervention group: Femilact synbiotic product (probiotic + prebiotic) with 30 oral capsules, gluten-free, containing a mixture of probiotic strains: Lactobacillus rhamnosus, Lactobaci

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Male gender Not having specific diseases such as autoimmune diseases, metabolic disorders and infectious and inflammatory diseases People with at least 1 year of futsal sports experience Having at least 2-3 futsal practice per week Being a permanent member of the team and registering one's profile in the national league. Declare agreement to participate in the plan and complete the plan's informed consent

Exclusion criteria

Exclusion criteria: Intolerance and sensitivity to synbiotics and similar products Taking antibiotics, painkillers, acute and chronic illness, acute and chronic illness medications or other medications in the last month Using drugs that affect lipid metabolism, such as cholesterol-lowering drugs, estrogen, progesterone, diuretics, niacin, tricyclic antidepressants, antiepileptic drugs (phenytoin, valproic acid, carbamazepine, and phenobarbital) and taking drugs that affect appetite and weight. Body, medicine to control blood sugar having specific muscle injuries and diseases such as myopathies (muscular dystrophy diseases); Neuropathies (Charcot-Marie-Tooth disease), nerve and muscle junction diseases (congenital myasthenia syndrome), motor neuron diseases (spinal muscular atrophy), fibromyalgia, myasthenia gravis before starting the study.

Design outcomes

Primary

MeasureTime frame
Serum creatine kinase levels. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Serum lactate dehydrogenase levels. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Serum troponin levels. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Serum aspartate aminotransferase levels. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Serum levels of IL-6. Timepoint: Before and after the intervention. Method of measurement: ELIZA KIT.;Serum levels of hsCRP. Timepoint: Before and after the intervention. Method of measurement: ELIZA KIT.;Serum levels of TNF-a. Timepoint: Before and after the intervention. Method of measurement: ELIZA KIT.;Anthropometric indices. Timepoint: Before and after the intervention. Method of measurement: Scale, Stadiometer,Tape.;Body composition indices. Timepoint: Before and after the intervention. Method of measurement: Impedance bio-electric system.;Dietary intake. Timepoint: Before and after the intervention. Method of measurement: Three-day food recall questionnaire.

Secondary

MeasureTime frame
Blood levels of fasting glucose. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Blood levels of fasting insulin. Timepoint: Before and after the intervention. Method of measurement: ELIZA KIT.;Serum levels of HbA1c. Timepoint: Before and after the intervention. Method of measurement: Spectrophotometry.;Blood levels of triglycerides. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Blood levels of total cholestrol. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Blood levels of HDL-cholesterol. Timepoint: Before and after the intervention. Method of measurement: Enzymatic method.;Blood levels of LDL-cholestrol. Timepoint: Before and after the intervention. Method of measurement: Friedewald formula.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBahram Pourghassem Gargari

Tabriz University of Medical Sciences

pourghassemb@tbzmed.ac.ir+98 41 1435 7580

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Apr 23, 2026