Nicorandil in Atherosclerosis Risk in Patients With Rheumatoid Arthritis
- NCT ID
- NCT07800351
- Registry status
- Not yet recruiting
- Study type
- Not specified in the registry data
- Phase
- Phase 3
- Sponsor
- Tanta University
Overview
ClinicalTrials.gov lists this study as Not yet recruiting.
Enrollment: 46 participants (Estimated).
What is being studied
No interventions are listed in the registry data.
Who may be eligible
- Ages
- Not specified in the registry data
- Sex
- Not specified in the registry data
- Healthy volunteers accepted
- No
ClinicalTrials.gov lists the following eligibility criteria.
Inclusion Criteria:
1. Adults aged 18-70 years, diagnosed with rheumatoid arthritis (RA) according to the 2010 ACR/EULAR classification criteria.
2. Receiving conventional synthetic disease-modifying antirheumatic drug (csDMARD) therapy for at least 3 months.
3. Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Exclusion Criteria:
1. Chronic autoimmune disease other than rheumatoid arthritis.
2. RA patients receiving biological DMARDs (bDMARDs).
3. Patients on lipid-lowering drugs (e.g., statins, fibrates).
4. Patients with metabolic or endocrine disease (e.g., diabetes mellitus, dyslipidemia).
5. Severe renal or hepatic impairment.
6. Any history of malignancy.
7. Current pregnancy or breastfeeding.
8. Current acute or chronic infection.
9. Currently participating in or has participated in a study of an investigational agent or device within 30 days prior to screening.
10. Known hypersensitivity or allergy to nicorandil or any of its components.
Study locations
1 study location is listed.
Site recruitment status is not specified in the registry data for these locations.
Countries: Egypt
- Gharbia Governorate, Egypt: 1
Sample of listed locations
- Rheumatology, Rehabilitation and Physical Medicine department -Tanta university hospitals — Tanta, Gharbia Governorate, 31511, Egypt — Site recruitment status not specified in the registry data
Study details
- Start date
- September 1, 2026
- Primary completion date
- February 1, 2027
- First posted
- September 2, 2026
Source and update information
- Source
- ClinicalTrials.gov
- NCT ID
- NCT07800351
- Registry last updated
- September 11, 2026
- QualifiedStudies registry data refreshed
- September 21, 2026
View NCT07800351 on ClinicalTrials.gov
Trial information can change. Confirm current study details with the study team or the registry.
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