Last updated: January 11, 2024
Sponsor: aya ramadan ashmawy sarhan
Overall Status: Active - Not Recruiting
Phase
3
Condition
Diabetes And Hypertension
Hormone Deficiencies
Diabetes Mellitus, Type 2
Treatment
Paroxetine
Placebo
Clinical Study ID
NCT06203275
paroxetine in type 2 diabetes
Ages 20-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients with established diagnosis of type 2 diabetes.
- Patients with type 2 diabetes treated with metformin based combined oral hypoglycemic ( metformin plus DDP4 inhibitor or metformin plus sulfonylureas or metformin plusGLP-1 analogues)
- Glycated hemoglobin (HbA1c) ≥ 7% and ≤9
- Age between 20 and 65 years
- BMI ≥25 kg/m2
Exclusion
Exclusion Criteria:
- Pregnant and lactating women
- Patients with diabetes complications except for hyperlipidemia if any.
- Patients with acute or chronic illness (such as flu, cancer, rheumatoidarthritis, etc….)
- Patients with renal impairment (S.Cr > 1.5 mg/dl) and hepatic impairment (Bilirubin level > 1.2 mg/dl).
- Patients with cardiovascular diseases
- Patients with condition that predispose to acidosis as COPD
- Patients with glaucoma
- Patients with thyroid disorders
- Patients on the medications that affect carbohydrate metabolism such as betablockers, contraceptives, thiazide diuretic, corticosteroids, sympathomimetic
- Patients treated with any oral anti-diabetes agents other oral hypoglycemicagents or treated with insulin
- Patients stabilized anticoagulants, antiplatelet, antipsychotics, MAOIs,amphetamines, NSAIDs, corticosteroids, ergotamine, levothyroxine, narcoticanalgesic, tramadol, liver microsomal enzyme inhibitors and liver microsomalenzyme inducers
Study Design
Total Participants: 44
Treatment Group(s): 2
Primary Treatment: Paroxetine
Phase: 3
Study Start date:
January 01, 2024
Estimated Completion Date:
January 31, 2026