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Effect of N-acetyl cysteine on Parkinson’s disease

Effect of N-acetyl cysteine as an adjuvant therapy on Symptoms and Progression of Parkinson’s disease

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20181006041247N1
Enrollment
40
Registered
2021-01-03
Start date
2019-04-09
Completion date
Unknown
Last updated
2021-02-22

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: Parkinson's disease patients receive N-acetylcysteine for one year. two times per day, every time 600 mg. The medicine is consumed after breakfast and after dinner

Sponsors

Sanandaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patient's informed consent No brain surgery in the patient's post medical history

Exclusion criteria

Exclusion criteria: having brain surgery within a year before starting the treatment period

Design outcomes

Primary

MeasureTime frame
The quality of the patient's movement skills and intellectual function. Timepoint: Before and after the invention (one year). Method of measurement: Filling the Unified Parkinson's Disease Rating Scale (UPDRS) questionnaire according to the patient's interview and examining.;Changes in dopaminergic areas within the patient's brain. Timepoint: Before and after the invention (one year). Method of measurement: Technetium-99m-Trodat-1 single-photon emission computerized tomography (SPECT).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArman Rahimmi

Sanandaj University of Medical Sciences

armanrahimmi@gmail.com+98 87 3316 2929

Outcome results

None listed

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