Screening and Management of Hyperuricemia in Patients with Chronic Medical Diseases in Assiut University Hospital
1 other identifier
observational
61
0 countries
N/A
Brief Summary
In this study, we aimed to evaluate patients with chronic medical diseases in Assiut university hospitals for -Detection of asymptomatic hyperuricemia .
- Early identification of associated comorbidities .
- Management of indicated hyperurecimia .
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Oct 2024
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
September 4, 2024
CompletedFirst Posted
Study publicly available on registry
September 19, 2024
CompletedStudy Start
First participant enrolled
October 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2025
CompletedSeptember 19, 2024
September 1, 2024
1 year
September 4, 2024
September 16, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
screening for asymptomatic hyperuricaemia
Detection of asymptomatic hyperuricemia patients with chronic medical diseases. Early identification of associated comorbidities . Management of indicated hyperurecimia .
baseline
Eligibility Criteria
The estimated minimum required sample size is 61 patients in one group
You may qualify if:
- Patients 18 years of age or older who were diagnosed with chronic medical diseases as diabetes mellitus , hypertension , obesity , metabolic syndrome , chronic kidney disease and cardiovascular disease (ischemic cardiomyopathy, heart failure ,coronary arteries disease) .
You may not qualify if:
- patients under the age of 18.
- patients kown to have gouty arthritis
- patients with acute kidney disease .
- patients receiving thiazide diuretics.
- patients with tumour lysis syndrome .
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Huda Abdelkader Khalafallah
Assiut University
- STUDY DIRECTOR
Mohammed Abbas Sobh
Assiut University
- STUDY DIRECTOR
Ayat Salah Ahmed
Assiut University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Year
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principal investigator
Study Record Dates
First Submitted
September 4, 2024
First Posted
September 19, 2024
Study Start
October 1, 2024
Primary Completion
October 1, 2025
Study Completion
November 1, 2025
Last Updated
September 19, 2024
Record last verified: 2024-09