RecruitingNCT06417138

Comparative Effectiveness of Different Drugs Used to tr€at Patients in Rheumatoid Arthritis Saudi Database (RASD)"

Comparative Effectiveness of Different Drugs Used to Treat Patients in Rheumatoid Arthritis Saudi Database (RASD) The Primary Objective of This Study is to Compare the Effectiveness of Different Biological Disease Modifying Antirheumatic Drugs (bDMARDs) and Targeted Synthetic (tsDMARDs) Using DAS-28-CRP and CDAI Scores.


Sponsor

Umm Al-Qura University

Enrollment

800 participants

Start Date

Dec 15, 2023

Study Type

OBSERVATIONAL

Conditions

Summary

Comparative effectiveness of different drugs used to treat patients in Rheumatoid Arthritis Saudi database (RASD) The goal of this observational study is to compare the effectiveness of different biological Disease Modifying Antirheumatic Drugs (bDMARDs) and targeted synthetic (tsDMARDs) using Disease Activity Score - 28 joints - C-Reactive Protien (DAS-28-CRP) and Clinical Disease Activity Index (CDAI) scores. In rheumatoid arthritis patients in Saudi Arabia who are part of Rheumatoid Arthritis Saudi Database (RASD). The main question\[s\] it aims to answer: * What is the most effective drug (biologocal or targeted synthetic) disease modifying antirheumatic drug used to treat rheumatoid arthritis in Saudi Arabia? * We are going to use two outcome mesures: Disease Activity Score - 28 joints - C-Reactive Protien (DAS-28-CRP) and Clinical Disease Activity Index (CDAI) scores Researchers will compare the treatment of rheumatoid arthritis using specific outcome measures in Rheumatoid Arthritis in Saudi Arabia. * Participants will be enrolled after a signed written concent in our Rheumatoid Arthritis Saudi Databas (RASD). * Their treatment data will used to compare the effectiveness of different drugs they are using.


Eligibility

Min Age: 18 Years

Inclusion Criteria5

  • All those patients who are age of 18 years and above and
  • meeting 2010 American College of Rheumatology classification criteria for rheumatoid arthritis.
  • Both male and female gender will be included.
  • There should be minimum of 12 months follow up with at least 3 documented visits of these patients to health care facilities.
  • Any patient who cannot recall the exact date of starting his drugs will be excluded during data analysis.

Interventions

OTHERbiological and targeted synthetic disease modifying anti rheumatic drugs (bDMARDs) and (tsDMARDs)

This is a registry-based study. It is an observational, retrospective trial. There is/are no interventional drug(s).


Locations(1)

International medical center

Jeddah, Mecca Region, Saudi Arabia

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NCT06417138


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