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The effect of N-acetylcysteine in the treatment of multiple sclerosis

Effect of N-acetylcysteine on nitric oxide, oxidative stress biomarkers, depression and stress in patients with multiple sclerosis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180515039662N1
Enrollment
60
Registered
2018-06-03
Start date
2018-06-20
Completion date
Unknown
Last updated
2018-07-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

multiple sclerosis. Multiple sclerosis

Interventions

Intervention 1: Intervention group: 30 ptients with multiple sclerosis will received 600 mg N-acetylcysteine effervescent tablet ( Zambon Pharma Co, Switzerland) twice daily within 12 hours (1200 mg d

Sponsors

Ahvaz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with multiple sclerosis more than 2 years EDSS = 4/5 Patients without current diagnosis of other inflammatory or autoimmune disease The age range is between 18-60 years Not taking depression or anxiety drugs Score of 10-30 (mild to moderate depression) from Beck Depression questionnaire in depression subscal and 15-25 (mild to moderate anxiety) from DASS21 questionnaire Tendency to participate in the study

Exclusion criteria

Exclusion criteria: Clinical relapses within 3 months before or during the study Pregnancy and lactation Cardiovascular diseases Patients with blood pressure disorders Liver and kidney disease Bronchospasm, asthma and any respiratory failure Gastric ulcer Bleeding and impaired blood coagulation Those who are allergic to NAC and any combination it contains, Taking antioxidants or NAC over the past 60 days Smoking, alcohol or drugs abuse Stressful events during the study

Design outcomes

Primary

MeasureTime frame
Glutathione. Timepoint: The beginning of the study- The end of the study. Method of measurement: Spectrophotometry.;Malondialdehyde. Timepoint: The beginning of the study- The end of the study. Method of measurement: Spectrophotometry.;Total antioxidant capacity. Timepoint: The beginning of the study- The end of the study. Method of measurement: Spectrophotometry.;Nitric oxide. Timepoint: The beginning of the study- The end of the study. Method of measurement: Spectrophotometry.;Depression. Timepoint: The beginning of the study- The end of the study. Method of measurement: Beck questionnaire.;Anxiety. Timepoint: The beginning of the study- The end of the study. Method of measurement: DASS 21 questionnaire.

Secondary

MeasureTime frame
Body Mass Index. Timepoint: The beginning of the study- The end of the study. Method of measurement: Body weight / hight square (kg/m2).;Dietary intake. Timepoint: The beginning of the study- The end of the study. Method of measurement: Three-day record.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactGolsa Khalatbari Mohseni

Ahvaz University of Medical Sciences

Khalatbari.g@ajums.ac.ir-

Outcome results

None listed

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