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N-acetylcysteine in Rheumatoid Arthritis

Evaluation the Effect of N-acetylcysteine on Inflammatory Biomarkers and Disease Activity Score (DAS28-ESR) of Rheumatoid Arthritis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190626044030N1
Enrollment
76
Registered
2019-12-25
Start date
2019-07-23
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

Rheumatoid arthritis.

Interventions

Intervention 1: Intervention group: The routine DMARDs in addition to 600 milligrams of effervescent of n-acetylcysteine(osve pharmaceutical company), twice daily for two months. Before intervention,

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Rheumatoid arthritis patients with a DAS28-ESR score>=2.6 No history of consuming antioxidant supplements within last 2 months No change of the type and dose of patient's drugs in the last 1 month No recent infectious disease Patients that are under treatment with DMARDs

Exclusion criteria

Exclusion criteria: Biologic agents therapy in the last 6 months Patients with concurrent autoimmune, rheumatoid disease and gout Using other complementary and alternative medicine Pregnancy and lactation Any addiction to psychotropic agents and opioids Uncontrolled hypertension Active gastrointestinal ulcer History of severe skin allergy Consuming nitroglycerin

Design outcomes

Primary

MeasureTime frame
IL-1, IL-17, DAS28-ESR, patient global assessment. Timepoint: Base, the end of the fourth week, the end of the eighth week. Method of measurement: Serum level, clinical signs, DAS28-ESR questionnaire.

Secondary

MeasureTime frame
ESR, Number of tender joints, number of swollen joints, reduced or increased need for oral or injectable corticosteroids. Timepoint: Baseline, at the end of the fourth week, at the end of the eighth week. Method of measurement: Serum level, clinical examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJamshid Salamzadeh

Shahid Beheshti University of Medical Sciences

j.salamzadeh@yahoo.com+98 21 2243 9982

Outcome results

None listed

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