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Comparison of the effectiveness of duloxetine and nortriptyline in the treatment of pain in rheumatoid arthritis patients

Phase 3
Recruiting
Conditions
pain.
Registration Number
IRCT20220901055848N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
54
Inclusion Criteria

Confirmation of the clinical diagnosis of mild to moderate Rheumatoid Arthritis by a rheumatologist
Presence of RF or AntiCCP in the serum of patients
Patients under treatment with methotrexate, prednisolone and hydroxychloroquine
Articular involvement without extra-articular involvement
Age range from 18 to 70 years
Pain complaint
Consent to participate in the study

Exclusion Criteria

The presence of major psychiatric disorders, including depression, anxiety disorders, bipolar, schizophrenia, abuse of any substance and medication.
History of allergy to Duloxetine or Nortriptyline
Pregnancy, breastfeeding, or planning to become pregnant in the near future
Refusing to consent to receive treatment according to the instructions of this protocol

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain level. Timepoint: Pain measurement before, 1 month, 2 months and 3 months after the start of taking one of the two drugs Nortriptyline and Duloxetine. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
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