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Effects of Probiotics on Constipation & Symptoms of Parkinson Disease

Evaluating the Efficacy of Probiotics in Constipation & Motor Dysfunctions in patients with Idiopathic Parkinson Disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170608034390N11
Enrollment
30
Registered
2022-05-14
Start date
2022-06-22
Completion date
Unknown
Last updated
2022-05-30

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

Conditions

Parkinson's Disease. Parkinson's disease

Interventions

The intervention group will take an oral capsule containing probiotics for 8 weeks before going to bed. Both groups will receive nutritional training and non-pharmacological strategies for treating co

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with Idiopathic Parkinson Disease With Rome IV criteria for functional constipation Age equal to or above 60 years Agreed to sign the informed written consent

Exclusion criteria

Exclusion criteria: There is a contraindication to probiotics, such as previous allergies to it Patients with active infection diagnosis Patients being treated with antibiotics. Patients less than 60 years Patients receiving other probiotics Patients who regularly use laxatives Patients who are immunocompromised Patients who are receiving traditional medicine products to relieve constipation. Patients who are receiving drugs that have a high risk of constipation in the complication profile with a high risk of 10%. (Except for FDA approved drugs in the treatment of Parkinson's)

Design outcomes

Primary

MeasureTime frame
Number of defecation per week. Timepoint: The beginning of the study and the end of the study. Method of measurement: Defecation booklet.

Secondary

MeasureTime frame
Unified Parkinson's Disease Rating Scale (UPDRS). Timepoint: The beginning of the study and the end of the study. Method of measurement: Unified Parkinson's Disease Rating Scale (UPDRS) Questionnaire.;Defecation consistency. Timepoint: The beginning of the study and the end of the study. Method of measurement: Bristol stool scale.;Sensation of complete evacuation. Timepoint: The beginning of the study and the end of the study. Method of measurement: Defecation booklet.;Frequency of medication interventions to improve constipation. Timepoint: The beginning of the study and the end of the study. Method of measurement: Defecation booklet.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHadi Esmaily

Shahid Beheshti University of Medical Sciences

esmaily_hadi@sbmu.ac.ir+98 21 8887 3704

Outcome results

None listed

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