Efficacy and safety of incorporating sodium-glucose Cotransporter-2 inhibitors to regimens of patients with type 2 diabetes
NCT ID NCT06268977
First seen Sep 10, 2026 · Last updated Sep 10, 2026
Summary
To detect the efficacy of SGLT2i in improving the metabolic parameters in patients with type 2 diabetes. \- To detect the side-effects of SGLT2i
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
482 people
The number who actually took part.
- Started
-
Apr 2025
- Finished
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Jan 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adults (≥18 years) 2. both genders ( male and female) 3. type 2 diabetic patients Exclusion Criteria: 1. history of severe hypoglycemia 2. patients with history of weight loss 3. Patients with history of recurrent UTI 4. patients already receiving SGLT2i as part of their treatment 5. very high blood glucose (A1c more than 11%) or presenting at the clinic with BG above 300 mg/dL. 6. clinical evidence of dehydration. 7. Frailty.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Assiut University Hospital
Asyut, Egypt
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