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RECRUITING
NCT07730723
PHASE2/PHASE3

The Effect of Nicorandil on Rheumatoid Arthritis Patients

Sponsor: Ain Shams University

View on ClinicalTrials.gov

Summary

The aim of this clinical trial is to determine whether nicorandil works in minimizing disease severity in patients with rheumatoid arthritis. The study will also assess the safety and tolerability of nicorandil. The main questions it aims to answer are: * Could nicorandil improve disease severity and symptoms of rheumatoid arthritis? * Does nicorandil lower the number of times participants need to use pain relieve medications? * Does the nicorandil improve participants functionality and ability to carry out daily activity? * Does nicorandil correct disease-associated damage and inflammation? * What side effects do participants have when taking nicorandil? Researchers will compare nicorandil to a placebo (a look-alike substance that contains no drug) to see if nicorandil works to decrease symptoms and severity of rheumatoid arthritis. Participants will: * Take nicorandil or a placebo two times daily for 3 months * Visit the clinic once every month for checkups * Keep a diary of their symptoms and the number of times they use a pain reliever

Official title: The Effect of Nicorandil on Disease Activity in Rheumatoid Arthritis Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

70

Start Date

2026-09-06

Completion Date

2027-07

Last Updated

2026-09-16

Healthy Volunteers

No

Interventions

DRUG

Nicorandil Oral Tablet

Nicorandil 10 mg oral tablets will be taken as one tablet twice daily for 3 months (12 weeks).

DRUG

Placebo

Placebo oral tablets will be taken as one tablet twice daily for 3 months (12 weeks).

DRUG

conventional synthetic antirheumatic drugs (cDMARDs)

A single or combination of cDMARDs and dose depend on disease severity.

Locations (1)

Ain Shams University Hospitals

Cairo, Abbasia, Egypt