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

Evaluating the Efficacy of Crocin on Movement Disorders and Neuronal Oxidative Stress of Parkinson's Disease; A Double-blind, Randomized, Placebo-controlled Clinical Trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170608034390N12
Enrollment
54
Registered
2022-12-09
Start date
2022-11-22
Completion date
Unknown
Last updated
2023-02-07

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

Intervention 1: Intervention group: Patients will take an oral capsule containing 30 mg of crocin in the morning and evening for 8 weeks. Granules containing crocin were obtained from Sami Saz Pharmac

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 80 Years

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
Unified 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

MeasureTime frame
Malondialdehyde reduction in blood (oxidative stress biomarker). Timepoint: The beginning of the study and the end of the study. Method of measurement: Spectrophotometry.

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