Anti-rheumatic Drug Use and Risk of COVID-19 Infection in Rheumatoid Arthritis Patients

NCT ID: NCT04434118

Last Updated: 2022-05-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Study Classification

OBSERVATIONAL

Study Start Date

2020-03-20

Study Completion Date

2021-12-30

Brief Summary

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Rheumatoid arthritis (RA) patients have an underlying immune deficiency and typically treated with immunosuppressive drugs, which may increase the risk of COVID-19 infection. Hydroxychloroquine (HCQ) has been found to possess antiviral activity against COVID-19. Thus, the aim of this study to investigate the ability of HCQ to reduce the risk of COVID-19 among RA patients.

Detailed Description

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Conditions

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Rheumatoid Arthritis COVID

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Rheumatoid Arthritis with COVID-19

Traditional antirheumatic drugs

Intervention Type DRUG

Hydroxychloroqine, Methotrexate, Glucocorticoids, Leflunomide, and Sulphasalazine

Rheumatoid Arthritis without COVID-19

Traditional antirheumatic drugs

Intervention Type DRUG

Hydroxychloroqine, Methotrexate, Glucocorticoids, Leflunomide, and Sulphasalazine

Interventions

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Traditional antirheumatic drugs

Hydroxychloroqine, Methotrexate, Glucocorticoids, Leflunomide, and Sulphasalazine

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

\- Data of all definite cases of RA were collected and reviewed from complete medical records of patients by a team that included 2 trained physicians using a pretested data collection form.

Exclusion Criteria

* Patients with acute lethal organ injury (e.g., acute myocardial infarction, acute coronary syndrome, acute pulmonary embolism, or acute stroke)
* Patients with decompensated or end stage chronic organ dysfunction (e.g., decompensated cirrhosis, decompensated chronic renal insufficiency, or severe congestive heart failure), diabetes mellitus, data of pregnant females, acquired immune deficiency syndrome (aids), and leukemia or other malignancies.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Sadat City University

OTHER

Sponsor Role lead

Responsible Party

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Mahmoud Samy Abdallah

Lecturer of Clinical Pharmacy, PhD.

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Faculty of Medicine

Shibīn al Kawm, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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IRB: RC-5-2020

Identifier Type: -

Identifier Source: org_study_id

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