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Effect of omega-3 plus vitamin E supplementation in treatment of patients with Parkinson's

Phase 2
Conditions
Parkinson disease.
Parkinson disease
Registration Number
IRCT2017061234497N1
Lead Sponsor
Kashan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Patients with Parkinson's; aged 50 to 80 years.

Exclusion Criteria

Subjects who were already taking omega-3 and/or vitamin E
Subjects who were taking DDP4 inhibitors, statins and anti-inflammatory drugs
Subjects who had depression and had severe psychosis.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Tumor necrosis factor alpha. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Interleukin-1. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Interleukin-8. Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.
Secondary Outcome Measures
NameTimeMethod
Peroxisome proliferator–activated receptor ? (PPAR?). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.;Low Density Lipoprotein Receptor (LDLR). Timepoint: At the beginning of the study and after 12 weeks of intervention. Method of measurement: PCR.
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