- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05847400
Predictors of Chronic Kidney Disease Among Type 2 Diabetic Patients in Assiut University Hospitals (Ckd&dm)
Study Overview
Status
Conditions
Detailed Description
Globally, the total number of people with diabetes is estimated to increase from 415 million (8.8%) in 2015 to 642 million (10.4%) in 2040, with the largest alterations expected to occur in the urban population of low- to middle-income countries (LMICs)1. Of them, type 2 diabetes mellitus (T2DM) accounts for more than 90% of people with diabetes2,3. By 2040, the difference worldwide is projected to broaden, with 477.9 million affected people living in urban areas and 163.9 million in rural areas1. It has been postulated that the burden of diabetes and its complications in the LMICs may be contributed by the economic development and rapid urbanisation via increased caloric intake and the adoption of a sedentary lifestyle2,4,5. More importantly, the most striking demo graphic change to diabetes prevalence in global terms also seems to be related to the growth of the proportion of the elderly population6. Despite rates of diabetes-related complications such as CVDs decreasing significantly in the past two decades, it has not translated nearly as well as kidney complications7. Approximately 10% of deaths in people with T2DM are attributable to kidney failure8. It is well-established that diabetes-related chronic kidney disease (CKD) is the leading cause of end-stage kidney disease (ESKD) in T2DM patients worldwide9,10.
In our study, we aim to identify and classify patients attending diabetic outpatient clinic with both CKD and
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Muhammed Al Abualsaud
- Phone Number: +20 106 923 9438
- Email: Aboalsaud25@gmail.com
Study Contact Backup
- Name: Peter At Munir
- Phone Number: 01553529181
Study Locations
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-
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Assiut, Egypt, 088
- Recruiting
- Assiut
-
Contact:
- Peter At Munir
- Phone Number: 01553529181
-
Contact:
- Muhammed Al Abualsaud, Master
- Phone Number: +20 106 923 9438
- Email: Aboalsaud25@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients with T2DM aged 18 years or older. For patients whom eGFR values < or =60 ml/min/1.73m2.
Patient with type 2 DM and ESRD on regular HD with duration less than 1 year
Exclusion Criteria:
Having kidney transplantation incomplete data on glycemic control. Patients with type 2 DM and ESRD on regular HD with duration more than 1 year. Pregnant woman. Patients with advanced comorbides(cardiac, hepatic,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
|---|
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CKD patients with T2DM on regular HD
CKD patients with T2DM attending Assuit university diabetic outpatients clinic and ESRD on regular HD at dialysis unit of Assuit University Hospital
|
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CKD patients with T2DM not on regular HD
CKD patients with T2DM attending Assuit university diabetic outpatients clinic and ESRD not on regular HD at dialysis unit of Assuit University Hospital
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
predictors of CKD among T2DM patients attending Assiut University Hospitals. To classify our patients into stages according to KDIGO guidelines
Time Frame: 3 years
|
To identify predictors of CKD among T2DM patients attending Assiut University Hospitals. To classify our patients into stages according to KDIGO guidelines |
3 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
the possible risk factors contributing to progessing CKD in T2DM patients.
Time Frame: 3 years
|
To identify the possible risk factors contributing to progessing CKD in T2DM patients.
|
3 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Muhammed Al Abualsaud, Assiut University
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ckd in tybe 2 dm
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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