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
45 participants
INTERVENTIONAL
2018-10-01
2026-12-01
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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Control group
No intervention
No interventions assigned to this group
Angiotensin receptor blockers
ARB ( Angiotensin receptor blockers) + Traditional therpy.
Angiotensin receptor blockers
Candesartan
Statins
Statin + Traditional therapy.
Statins
Atorvastatin
Interventions
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Angiotensin receptor blockers
Candesartan
Statins
Atorvastatin
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Hepatic or renal impairment.
18 Years
65 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
Prof of Clinical Pharmacy
Emad M Elshebini, MD
Role: STUDY_CHAIR
Rheumatology Dept. - Menoufia University
Ahmed HM El-Abd, 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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Ahmed El-Abd, Msc
Role: primary
Other Identifiers
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Rheumatoid
Identifier Type: -
Identifier Source: org_study_id