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临床试验/NCT05748925
NCT05748925已完成4 期

Study of the Cardio Renal Effects of SGLT2 Inhibitors Among Diabetic and Non-diabetic Lupus Nephritis Patients

Mansoura University1 个研究点 分布在 1 个国家目标入组 84 人开始时间: 2022年10月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
84
试验地点
1
主要终点
Effect of Dapagliflozin Compared to Placebo on Renal Function After One Year

研究概览

简要总结

This study aims to assess sodium glucose linked transoprter inhibitors(SGT2i) role in regression of ongoing kidney and cardiac diseases among lupus nephritis patient either diabetic or non-diabetic under different immunosuppressive therapy.

The main objective of this study is to:

To compare use of sodium glucose linked transoprter inhibitors (SGLT2i) versus standard care in regression of chronic kidney disease in patient with lupus nephritis (LN).

To study the safety and efficacy of this drug group with use of immunosuppression and possible interaction.

Patients with an estimated glomerular filtration rate (eGFR) >30 ml/min/1.73m2 will be randomized into two groups Study group will receive SGLT2i inhibitor as add on drug or replace another drug according to patient clinical situation, Dapagliflozin 10 mg and 25 mg will be used once daily with or without food.

Control group will be maintained on placebo.We will follow up all patients for 12 months and compare their results.

详细描述

Study sitting:

Nephrology and renal transplant unit at urology and nephrology center in Mansoura University.

It will include 100 patients with lupus nephritis, Diagnosis of glomerulonephritis was performed by renal biopsy, and all of the renal biopsies were carried out at urology and nephrology center.

Patients with an estimated glomerular filtration rate (eGFR) >30 ml/min/1.73m2 will be randomized into two groups Study group will receive SGLT2i inhibitor as add on drug or replace another drug according to patient clinical situation, dapagliflozin 10 mg and 25 mg will be used once daily with or without food.

Control group will be maintained on placebo. The primary endpoint will be sustained decline in eGFR ≥50%, ESKD, or kidney or cardiovascular death We will follow up all patients for 12 months and compare their results.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double (Participant, Care Provider)

盲法说明

double blind

入排标准

年龄范围
16 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged more than 16 year.
  • Willing to sign informed consent.
  • Diagnosis of SLE according to EULAR/ACR classification criteria.
  • Renal biopsy showed lupus nephritis.
  • Patient with eGFR > 30 ml/min/1.73m2 by cockcroft-gault equation.

排除标准

  • Patients with eGFR <30 ml/min per 1.73 m
  • Current pregnancy or lactation.
  • Medical history of chronic disease (CLD, cancer, severe respiratory distress, gastrointestinal tract lesions).
  • Patients refusing to participate in the study or lost follow up.
  • Evidence of urinary obstruction of difficulty in voiding at screening.
  • Patients who are receiving high dose diuretics or combined ACEI, Angiotensin II receptor blockers (ARBS).
  • Patients who have frequent hypotensive episode or SBP <100 mmHg.

研究组 & 干预措施

study group

Active Comparator

study group: will receive SGLT2i as add on drug or replace another drug according to the patient clinical situation, Dapagliflozin 10 mg will be used once daily with or without food for one ye

干预措施: dapagliflozin (Drug)

control group

Active Comparator

Control group: will receive placebo as add on drug once daily with or without food for one year.

干预措施: placebo (Drug)

结局指标

主要结局

Effect of Dapagliflozin Compared to Placebo on Renal Function After One Year

时间窗: one year

Effect of dapagliflozin compared to placebo on eGFR,24- hour urinary protein

Cardiovascular Assessment in Two Groups

时间窗: 1 year

Coronary artery calcification will be measured using non-contrast computed tomography (NCCT). The Agatston score, a standardized method for quantifying coronary calcification, will be used to assess and compare baseline and 1-year follow-up measurements between the dapagliflozin and placebo groups.

Effect of Dapagliflozin Compared to Placebo on Erythropoietin Level

时间窗: 1 year

Erythropoietin level will be measured in two groups before and after intervention

Effect of Dapagliflozin Compared to Placebo on Hepcidin Level

时间窗: 1 year

hepcidin level will be measured in two groups before and after intervention

Effect of Dapagliflozin Compared to Placebo on Renal Function

时间窗: 1 year

Effect of Dapagliflozin Compared to Placebo on Renal Function on uric acid after 1 year

次要结局

  • Effect of Dapagliflozin Compared to Placebo on ECCHO Parameters(1 year)
  • Effect of Dapagliflozin Compared to Placebo on Body Weight(1 year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Nourelsabah Mohamed

Nephrology specialist at mansoura urology and nephrology center

Mansoura University

研究点 (1)

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