Irisin Hormone as a Novel Diagnostic Marker for Detection and Progression of Diabetic Nephrophathy Patients
Evaluation of Irisin as a Novel Diagnostic Marker for Early Detection and Progression of Diabetic Nephrophathy
1 other identifier
observational
200
0 countries
N/A
Brief Summary
Study the relation between irisin level and progression of diabetic nephropathy and its early detection.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Apr 2026
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
February 20, 2026
CompletedFirst Posted
Study publicly available on registry
February 27, 2026
CompletedStudy Start
First participant enrolled
April 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
March 1, 2028
March 10, 2026
February 1, 2026
11 months
February 20, 2026
March 7, 2026
Conditions
Outcome Measures
Primary Outcomes (1)
Measure number of Participants With Diabetic nephropathy Adverse healthy people as Assessed by irisin hormone ).
Participants With Diabetic nephropathy Adverse healthy people as Assessed by irisin hormone ).
Two years
Interventions
Eligibility Criteria
Type 2 diabetic patients between 30-75 years old
You may qualify if:
- Type 2 diabetic patients
You may not qualify if:
- Non-diabetic kidney diseases.
- Acute illness, infection, obesity, hypertension, type 1 DM.
- Malignancy, other endocrine disorders, corticosteroid drugs, pregnancy, lactation.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Ahmed Se Mahmoud, ass prof
Sohag University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 2 Months
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principle investigator
Study Record Dates
First Submitted
February 20, 2026
First Posted
February 27, 2026
Study Start
April 1, 2026
Primary Completion (Estimated)
March 1, 2027
Study Completion (Estimated)
March 1, 2028
Last Updated
March 10, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will not share