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Evaluating the Efficacy of Crocin on Movement Disorders and Neuronal Oxidative Stress of Parkinson's Disease

Phase 3
Recruiting
Conditions
Parkinson's disease.
Parkinson's disease
Registration Number
IRCT20170608034390N12
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
54
Inclusion Criteria

Idiopathic Parkinson's patients
Age 30 to 80 years
No change in diet, medication and supplements during 8 weeks
They declare their agreement to participate in the clinical trial through a written consent form

Exclusion Criteria

Patients with a history of saffron allergy
Patients with severe episodes of wearing off
Consumers of saffron more than 1 gram per day
Taking warfarin, monoamine oxidase inhibitors
Pregnant and lactating patients
Liver disease
Occurrence of urticaria complications; skin itching; Nausea and vomiting and dizziness
Patients with severe Hoehn and Yahr stage 5 Parkinson's disease

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
nified Parkinson's Disease Rating Scale (UPDRS). Timepoint: At the beginning and eight weeks after the start of the study. Method of measurement: Unified Parkinson's Disease Rating Scale (UPDRS) Questionnaire.
Secondary Outcome Measures
NameTimeMethod
Malondialdehyde reduction in blood (oxidative stress biomarker). Timepoint: The beginning of the study and the end of the study. Method of measurement: Spectrophotometry.
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