Clinical trial

Effect of Sodium-Glucose Co-transporter 2 Inhibitors on Kidney Disease Progression and Bone Mineral Metabolism in Non-diabetic Patients With Chronic Kidney Disease

Name
MD.22.02.600
Description
It is a randomized controlled trial in which 100 non diabetic chronic kidney disease (CKD) patient is being participated. Their estimated glomerular filtration rate (eGFR) between 25-75 ml/min/1.73 m2. Participants will be randomized into two groups: * Study group: includes 50 patients, they will receive Sodium glucose co-transporter 2 inhibitor (SGLT2i) as add on drug, Dapagliflozin 10 mg will be used once daily with or without food. * Control group: includes 50 patients, they will receive placebo their medication. The investigators will follow up all patients for 12 months and compare their results. This study aims to: 1. Assess SGLT2i role in delaying the progression of ongoing chronic kidney disease. 2. Study the impact of SGLT2i on bone and mineral metabolism in this patients' population.
Trial arms
Trial start
2022-11-10
Estimated PCD
2023-11-10
Trial end
2024-01-10
Status
Active (not recruiting)
Phase
Early phase I
Treatment
Dapagliflozin 10mg Tab
Dapagliflozin which is (SGLT2 inhibitor) will be used as add on medication.
Arms:
Dapagliflozin group
Other names:
Dapagliflozin
Placebo
Placebo which has the same shape as Dapagliflozin but without active ingredient will be used as add on medication for control group.
Arms:
Placebo group
Other names:
control
Size
100
Primary endpoint
Effect of dapagliflozin on CKD progression
1 year
Effect of dapagliflozin on Bone
1 year
Effect of dapagliflozin on minerals
1 year
Effect of dapagliflozin on BMD
1 year
Eligibility criteria
Inclusion Criteria: 1. Patients aged more than 18 year. 2. CKD patient with eGFR from 25 to 75 ml/min/1.73m2 with no evidence of acute drop of the GFR in the last 3 months. 3. Willing to sign informed consent. Exclusion Criteria: 1. eGFR less than 25 ml/min per 1.73 m2. 2. Medical history of chronic disease (diabetes mellitus, chronic liver and/or respiratory diseases). 3. Patients with primary or secondary glomerulonephritis/ nephrotic syndrome (proteinuria ≥ 3.5 gm/day) and/or any evidence of active immunological/ collagen vascular disease. 4. Inability to sign the study consent form or refusal to participate in the study. 5. Evidence of urinary obstruction. 6. Patients with evidence of volume depletion or receiving a combination of angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor blockers (ARBS).. 7. Patients with current history of frequent hypotensive episodes or systolic blood pressure \<100 mmHg. 8. Patients with history of recurrent urinary tract infection and/or valvovaginitis 9. Patients with ongoing active malignancy. 10. Patients with any evidence of active infection including human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV) and tuberculosis (TB). 11. Current or previous organ transplantation, or expected to get a kidney transplant within 12 months. 12. Patients who received any SGLT2i for more than 3 months in the past. 13. Patients who are already on medications that may affect or interact with bone metabolism such as bisphosphonates, calcitonin, steroid, denosumab and estrogen during the last 6 months. 14. Pregnant and/or lactating woman.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': '100 patients with non-diabetic CKD with an estimated glomerular filtration rate (eGFR) of 25-75 ml/min/1.73m2 will be randomized into two groups:\n\n* Study group: includes 50 patients, they will receive SGLT2i as add on drug, Dapagliflozin 10 mg will be used once daily with or without food.\n* Control group: includes 50 patients, they will receive placebo plus their medication.', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}}, 'enrollmentInfo': {'count': 100, 'type': 'ACTUAL'}}
Updated at
2023-02-21

1 organization

1 product

1 drug

3 indications

Indication
Bone Diseases
Indication
Metabolic