Paroxetine Safety and Efficacy in Rheumatoid Arthritis
- Disease/Condition
- Rheumatoid Arthritis
- Drug/Device/Intervention
- Methotrexate
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Mostafa Bahaa
- Funder
- Tanta University
- Location
- Damietta, Egypt
- Phase
- Phase 3
- Start date
- Jan 31, 2024
- End date
- Feb 20, 2026
- Enrollment
- 100 participants
The primary efficacy end point will be the change in the 28-joints disease activity score (DAS28).
Rheumatoid arthritis (RA) is a systemic chronic auto-inflammatory disorder which imposes a
 remarkable burden of morbidity and mortality on global health. The complex interaction
 between genetics, environment, and immunological response contribute to RA pathogenesis.
 Current treatment comprises conventional disease-modifying anti-rheumatic drugs (DMARDs)
 followed by biological DMARDs, if necessary, to achieve low disease activity or remission.
 Therapeutics used in RA had limitations in tolerability, access, and response duration and
 magnitude. Consequently, implementation of safe adjunctive treatment for RA is urgently
 needed to boost the therapeutic response.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06231745
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06231745 through Pure Global AI's free database. This Phase 3 trial is sponsored by Mostafa Bahaa and is currently Recruiting. The study focuses on Rheumatoid Arthritis. Target enrollment is 100 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.