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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05781711
Other study ID # 3-2023
Secondary ID
Status Recruiting
Phase Phase 2
First received
Last updated
Start date January 6, 2023
Est. completion date November 20, 2025

Study information

Verified date April 2024
Source Tanta University
Contact Mostafa M Bahaa, PhD
Phone 0201025538337
Email mbahaa@horus.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Parkinson's disease (PD) is one of the most common neurodegenerative diseases characterized by the progressive loss of dopaminergic (DA) neurons in the substantia nigra compacta (SNc) and aggregation of Lewy bodies in neurons. Although aging, oxidative damage and neuroinflammation have been recognized to play crucial roles in the pathogenesis of PD, the precise etiology remains obscure. Emerging evidence suggests PD is a systemic metabolic disease, and metabolic abnormality correlates with functional alternations in PD


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date November 20, 2025
Est. primary completion date September 20, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: Age = 18 years Both males and females will be included Negative pregnancy test and effective contraception. Diagnosed Parkinson's disease patient taking Levodopa Exclusion Criteria: Secondary causes of Parkinsonism Diabetic patients Patients taking anti-inflammatory drugs Atypical parkinsonian syndromes Prior stereotaxic surgery for Parkinson's disease Pregnancy and lactation Suffering from active malignancy Addiction to alcohol and/or drugs Known allergy to the studied medications

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
levodopa-carbidopa
levodopa-carbidopa is the standard therapy used in Parkinson's disease
Metformin
Metformin, a biguanide family member commonly used in treatment for type 2 diabetes, appears to increase liver and peripheral tissue sensitivity to insulin as well as reduce hepatic glucose production

Locations

Country Name City State
Egypt Faculty of Medicine, Menoufia University Tanta Shebeen El-Kom

Sponsors (4)

Lead Sponsor Collaborator
Tanta University Eman Ibrahim Elberri, Faculty of Pharmacy, Tanta University, Fedaa Abd El-monem Kamal El-deen Kotkata Faculty of Pharmacy, Tanta University, Manal Ali Mahrous Hamouda Faculty of Pharmacy, Menufia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary • The primary endpoint is the change in The Unified Parkinson's Disease Rating Scale (UPDRS) • The primary endpoint is the change in the Unified Parkinson's Disease Rating Scale (UPDRS 3 months
Secondary The secondary endpoint is estimated by changes in serum biomarkers. The secondary endpoint is estimated by changes in serum biomarkers such as brain derived neurotropic factor 3 months
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