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NOT YET RECRUITING
NCT07497282
PHASE2

Venlafaxine as Adjunct Therapy in Rheumatoid Arthritis

Sponsor: Ain Shams University

View on ClinicalTrials.gov

Summary

Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by persistent inflammation of the joints, leading to pain, swelling, disability, and reduced quality of life. Current therapies, although effective, may have limited efficacy or tolerability in some patients. Biological DMARDs are often associated with adverse effects, including increased risk of serious infections and heart failure. Long-term use may also increase the risk of malignancies. These limitations, together with their high cost. Venlafaxine, a serotonin-norepinephrine reuptake inhibitor (SNRI), has shown potential anti-inflammatory properties in addition to its antidepressant effects. This study aims to evaluate the efficacy and safety of venlafaxine as an adjunct therapy in the management of rheumatoid arthritis.

Official title: The Effect of Venlafaxine as an Adjunct Therapy on The Clinical Outcome of Rheumatoid Arthritis Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2026-03-26

Completion Date

2026-12-26

Last Updated

2026-03-27

Healthy Volunteers

No

Interventions

DRUG

venlafaxine extended-release (XR)

35 patients will receive the standard RA treatment in addition to venlafaxine extended-release (XR) initiated at a dose of 75 mg/day for one week to ensure tolerability, followed by an increase to 150 mg/day, which will be maintained for the duration of the study (12 weeks)

OTHER

Standard conventional Rheumatoid Arthritis Therapy

35 patients will receive the standard treatment of RA, which will be maintained for the duration of the study (12 weeks).