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Effect of N-Acetyl Cysteine in Rheumatoid arthritis

A Comparative study on efficacy and safety of N-Acetyl Cysteine as an add on therapy with standard therapy in patients with Rheumatoid arthritis- A Randomised Open Labelled Prospective study. - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063534
Enrollment
54
Registered
2024-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: M057- Rheumatoid arthritis with rheumatoid factor without organ or systems involvement

Interventions

Intervention1: N- ACETYL CYSTEINE: 600 mg twice a day for 12 weeks Control Intervention1: Methotrexate, Hydroxychloroquine: 7.5 mg / week 400 mg / day for 12 weeks

Sponsors

Government Kilpauk Medical College
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Newly diagnosed as rheumatoid arthritis within 2 years by ACR criteria and having DAS 28-ESR score more than 3.2 who are not responding to standard therapy

Exclusion criteria

Exclusion criteria: Newly diagnosed Rheumatoid arthritis patients having DAS 28-ESR score less than 3.2 History of Psychiatric illness or drug abuse History of seizure disorder. Known case of hypersensitive to N acetyl cysteine. Pregnant and lactating females History of any autoimmune disease other than rheumatoid arthritis Patient taken biological agent therapy in last 6 months Patients taking N acetyl cysteine for any other cause.

Design outcomes

Primary

MeasureTime frame
Disease activity assessed using DAS 28 ESR score and CRPTimepoint: at baseline and 12 weeks

Secondary

MeasureTime frame
particpants will be assessed by CBC,LFT, RFT,CRP, ESR, RFTimepoint: at baseline , 4 ,8,12, 16 weeks

Countries

India

Contacts

Public ContactDr T Aruna

Government Kilpauk Medical College

arunabala511@gmail.com9444276923

Outcome results

None listed

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