Semi-individualised Chinese medicine treatment as an adjuvant management for diabetic nephropathy: a pilot add-on, randomised, controlled, multicentre, open-label pragmatic clinical trial

被引:9
|
作者
Chan, Kam Wa [1 ]
Ip, Tai Pang [2 ]
Kwong, Alfred Siu Kei [3 ]
Lui, Sing Leung [2 ]
Chan, Gary Chi Wang [4 ]
Cowling, Benjamin John [5 ]
Yiu, Wai Han [1 ]
Wong, Dickson Wai Leong [1 ]
Liu, Yang [1 ]
Feng, Yibin [6 ]
Tan, Kathryn Choon Beng [7 ]
Chan, Loretta Yuk Yee [1 ]
Leung, Joseph Chi Kam [1 ]
Lai, Kar Neng [1 ]
Tang, Sydney Chi Wai [1 ]
机构
[1] Univ Hong Kong, Div Nephrol, Dept Med, Hong Kong, Hong Kong, Peoples R China
[2] Tung Wah Hosp, Dept Med, Hong Kong, Hong Kong, Peoples R China
[3] Queen Mary Hosp, Dept Family Med & Primary Healthcare, Hong Kong, Hong Kong, Peoples R China
[4] Queen Mary Hosp, Div Nephrol, Dept Med, Hong Kong, Hong Kong, Peoples R China
[5] Univ Hong Kong, Sch Publ Hlth, Div Epidemiol & Biostat, Hong Kong, Hong Kong, Peoples R China
[6] Univ Hong Kong, Sch Chinese Med, Hong Kong, Hong Kong, Peoples R China
[7] Univ Hong Kong, Div Endocrinol, Dept Med, Hong Kong, Hong Kong, Peoples R China
来源
BMJ OPEN | 2016年 / 6卷 / 08期
关键词
CHRONIC KIDNEY-DISEASE; SAMPLE-SIZE; FIBROSIS; RATS; EXPRESSION; INJURY;
D O I
10.1136/bmjopen-2015-010741
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Diabetes mellitus and diabetic nephropathy (DN) are prevalent and costly to manage. DN is the leading cause of end-stage kidney disease. Conventional therapy blocking the renin-angiotensin system has only achieved limited effect in preserving renal function. Recent observational data show that the use of Chinese medicine (CM), a major form of traditional medicine used extensively in Asia, could reduce the risk of end-stage kidney disease. However, existing clinical practice guidelines are weakly evidence-based and the effect of CM remains unclear. This trial explores the effect of an existing integrative Chinese-Western medicine protocol for the management of DN. Objective: To optimise parameters and assess the feasibility for a subsequent phase III randomised controlled trial through preliminary evaluation on the effect of an adjuvant semi-individualised CM treatment protocol on patients with type 2 diabetes with stages 2-3 chronic kidney disease and macroalbuminuria. Methods and analysis: This is an assessor-blind, add-on, randomised, controlled, parallel, multicentre, open-label pilot pragmatic clinical trial. 148 patients diagnosed with DN will be recruited and randomised 1:1 to a 48-week additional semi-individualised CM treatment programme or standard medical care. Primary end points are the changes in estimated glomerular filtration rate and spot urine albumin-to-creatinine ratio between baseline and treatment end point. Secondary end points include fasting blood glucose, glycated haemoglobin, brain natriuretic peptide, fasting insulin, C peptide, fibroblast growth factor 23, urinary monocyte chemotactic protein-1, cystatin C, nephrin, transforming growth factor-beta 1 and vascular endothelial growth factor. Adverse events are monitored through self-completed questionnaire and clinical visits. Outcomes will be analysed by regression models. Enrolment started in July 2015. Ethics and registration: This protocol is approved by the Institutional Review Board of the University of Hong Kong/Hospital Authority Hong Kong West Cluster (reference number UW 14-301).
引用
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页数:8
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