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Effect of probiotic in Parkinson's disease patients

Effect of ingestion of Iranian native multi-strain probiotic Supplement on inflammatory and oxidative stress factors in Parkinson's disease patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200921048793N1
Enrollment
30
Registered
2020-10-09
Start date
2020-08-22
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

parkinson. Parkinson's disease

Interventions

Intervention 1: Intervention group: probiotic capsule (Tak Gene Zist, Iran) containing L. rhamnosus, L. plantarum, L. acidophilus, L. salivarius, B. coagulans, B. longum ,vitamin D3 (400IU), magnesium

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Age over 18 and under 80 Diagnosis of idiopathic Parkinson's disease based on UK PD Society Brain Bank criteria Using l-dopa or dopaminergic agonist

Exclusion criteria

Exclusion criteria: Use of systemic antibiotics, antifungals, antivirals or antiparasitics (intravenous, intramuscular, or oral) Use of commercial probiotics: includes tablets, capsules. Major surgery of the GI tract, with the exception of cholecystectomy and appendectomy, in the past five years History of active uncontrolled gastrointestinal disorders or diseases including: inflammatory bowel disease (IBD) including ulcerative colitis (mild-moderate-severe), Crohn's disease (mild-moderate-severe), or indeterminate colitis Infectious gastroenteritis, colitis or gastritis, persistent or chronic diarrhea of unknown etiology, Clostridium difficile infection (recurrent) or Helicobacter pylori infection (untreated) Age over 80

Design outcomes

Primary

MeasureTime frame
Analyses Level of TNF-a, IL-1ß, IL-10, Malondialdehyde (MDA), Total antioxidant capacity (TAC). Timepoint: At the beginning of the study and week 12. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehri Salari

Shahid Beheshti University of Medical Sciences

mehri.salari@gmail.com+98 21 25719

Outcome results

None listed

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