The Effect of Sitagliptin, Pioglitazone and Dapagliflozine on Myocardial Infarction in Diabetic Rats
- Sponsor
- Al-Azhar University
- Study ID
- NCT07083232
- Phase
- PHASE4
- Status
- Completed
Conditions
- Diabetic
- Myocardial Infarction
Eligibility Criteria
- Sex
- MALE
- Age
- N/A - N/A
- Healthy Volunteers
- Not accepted
Interventions
- standard normal diet — DIETARY_SUPPLEMENTGroup I: formed of normal animals. They were allowed standard normal diet and water. They received no drugs
- low dose Streptozotocin — DRUGNon-treated diabetic rats; diabetes was induced by administration of 20% fructose solution in drinking water for 2 weeks, then intra peritoneal injection of a low dose STZ (40 mg/kg b.w.), was done
- Sitagliptin (Novartis, USA) — DRUGSitagliptin treated diabetic group sitagliptin was administered by gastric gavage in a dose 10mg/ kg /day for 4 weeks
- Pioglitazone hydrochloride (Unipharma., Egypt) — DRUGPioglitazone treated diabetic group (G4); Pioglitazone was administered by gastric gavage in a dose 10 mg/ kg /day for 4 weeks
- Dapagliflozine hemihydrate (Janssen, USA) — DRUGDapagliflozine treated diabetic group (G5); Dapagliflozine was administered by gastric gavage in a dose 1mg/ kg /day for 4 weeks
Study Details
The aim of the present study is to evaluate the prophylactic effect of Sitagliptin, Pioglitazone and Dapagliflozine on Isoprenaline induced myocardial infarction in type II diabetic rats.
Key Dates
- Start date
- Oct 30, 2024
- Status verified
- Jul 2023
- Primary completion
- Oct 30, 2024
- Completion
- Nov 30, 2024
Study Design
- Enrollment
- 50 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- PREVENTION
Arms
- Placebo Comparator: standard normal diet and water groupGroup I: formed of normal animals. They were allowed standard normal diet and water. They received no drugs.
- Experimental: low dose Streptozotocin groupGroup II: Non-treated diabetic rats; diabetes was induced by administration of 20% fructose solution in drinking water for 2 weeks, then intra peritoneal injection of a low dose STZ (40 mg/kg b.w.)
- Experimental: Sitagliptin groupGroup III: Sitagliptin treated diabetic group sitagliptin was administered by gastric gavage in a dose 10mg/ kg /day for 4 weeks
- Experimental: Pioglitazone groupGroup IV : Pioglitazone treated diabetic group ; Pioglitazone was administered by gastric gavage in a dose 10 mg/ kg /day for 4 weeks
- Experimental: Dapagliflozine groupGroup V : Dapagliflozine treated diabetic group (G5); Dapagliflozine was administered by gastric gavage in a dose 1mg/ kg /day for 4 weeks
Primary Outcome Measure
blood glucose [ Time Frame: one week ]
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