Study Results
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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RECRUITING
PHASE3
75 participants
INTERVENTIONAL
2018-10-01
2027-10-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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No intervention
No intervention
No interventions assigned to this group
Rupatadine
Rupatadine 10 mg once daily.
Rupatadine
Rupatadine 10 mg daily
Montelukast
Montelukast 10 mg daily
Montelukast
Montelukast 10 mg daily
Interventions
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Rupatadine
Rupatadine 10 mg daily
Montelukast
Montelukast 10 mg daily
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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Sherief Abd-Elsalam
OTHER
Responsible Party
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Sherief Abd-Elsalam
Ass. Prof. Tropical Medicine
Principal Investigators
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Sahar k Hegazy, Prof
Role: PRINCIPAL_INVESTIGATOR
Head of Clinical Pharmacy Department
Tarek M Mostafa, Prof
Role: STUDY_DIRECTOR
Clinical pharmacy Department- Tanta University
Salwa E Abd El-Ghany, Prof
Role: STUDY_CHAIR
Rheumatology Dept. - Tanta University
Fedaa AK Kotkata, Msc
Role: STUDY_CHAIR
Clinical pharmacy Department-Tanta University
Locations
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Sherief Abd-Elsalam
Tanta, , Egypt
Countries
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Central Contacts
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Facility Contacts
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Fedaa Kotkata, Msc
Role: primary
References
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Mostafa TM, Hegazy SK, El-Ghany SEA, Kotkata FAE. Comparative study evaluating antihistamine versus leukotriene receptor antagonist as adjuvant therapy for rheumatoid arthritis. Eur J Clin Pharmacol. 2021 Dec;77(12):1825-1834. doi: 10.1007/s00228-021-03181-2. Epub 2021 Jul 4.
Other Identifiers
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Rheumatoid Arithritis
Identifier Type: -
Identifier Source: org_study_id