Efficacy, Safety and Response Predictors of Adjuvant Astragalus Therapy for Diabetic Kidney Disease

Diabetic Kidney Disease Clinical Trial

— READY  

Official title:

Efficacy, Safety and Response Predictors of Adjuvant Astragalus Therapy for Diabetic Kidney Disease (READY) - An Open-label Randomised Controlled Trial With Responder Regression Analysis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03535935
• Other study ID #: RE-02
• Status: Recruiting
• Phase: Phase 2/Phase 3
• Start date: July 1, 2018
• Est. completion date: December 31, 2022

Study information

• Verified date: December 2020
• Source: The University of Hong Kong
• Contact: Sydney CW TANG, MD, PhD
• Phone: +852 22553879
• Email: scwtang[@]hku.hk
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This add-on open-label randomised controlled pragmatic trial aims to: 1. evaluate the effect of add-on astragalus treatment on type 2 diabetic patients with stage 2 to 3 chronic kidney disease and macroalbuminuria. 2. estimate treatment effect, variance, recruitment rate, attrition rate and change in clinical manifestation including Chinese medicine syndrome for parameters optimisation and feasibility assessment for a subsequent phase III randomised controlled trial. 3. assess response predictors for efficacy and safety among type 2 diabetic patients with stage 2 to 3 chronic kidney disease and macroalbuminuria receiving add-on astragalus treatment

Description:

This add-on open-label randomised controlled pragmatic trial. Sample size is calculated based on planned regression analysis. We believe an annual GFR benefit of 5 ml/min/1.73m2 is deemed significant clinically. 118 patients are therefore needed to offer a power of 70% to detect a GFR difference of 5 ml/min/1.73m2 over 48-week allowing 15% attrition rate for this study with a significance level of alpha equals to 0.05. A trial management committee (TMC) formed by PA, Co-As and RA will centralise all the data of the trial. Co-As and RA will collect, clean and send the data of patients to TMC on a weekly basis. All data will be double entered to computer and cleaned before analysis to prevent data entry errors. All data transfer will be encrypted to protect patients' confidentiality. TMC will have regular meetings monthly with experts to discuss the progress of the trial. An independent Data Monitoring Board (DMB) will be invited to monitor the progress of the trial. DMB will advise ethics committee to terminate the trial if data is showing extreme benefits or harm. Detailed guidelines will be discussed and set by DMB. Missing values will be imputed with last observation carried forward. Patient without a postrandomisation assessment for a particular efficacy endpoint will be excluded from the analysis of that endpoint. Regression analysis will be used to compare the adjusted mean of eGFR, UACR, HbA1c, FBG, and other biomarkers at week 48 between groups and statistical significance. The adverse events will be analysed in a narrative manner. The percentage of all adverse events and the rate of attrition due to adverse events will be compared between intervention groups and control groups. To minimise Type I error inflation, the analysis will follow a hierarchical approach in the order of 1) comparison of baseline to end of treatment on eGFR and UACR; 2) comparison of baseline to end of treatment on other outcome measurements; 3) comparison of baseline to treatment midpoints on eGFR and UACR and 4) comparison of baseline to treatment midpoints on other outcome measurements. Subgroup analysis will be performed for different age groups, gender chronic kidney disease stage and severity of albuminuria. The dependent variable is the treatment response which is categorised into: 1. Improved or stabilised renal function, defined as eGFR after 48-week treatment being higher or equal to baseline. 2. Non-responder, defined as patients having eGFR decreased at a rate of less than 5 mL/min/1.73m2 after 48-week treatment compared to baseline. 3. Rapid deteriorating renal function, defined as eGFR of more than 5 mL/min/1.73m2 after 48-week treatment compared to baseline. Potential prognostic variables (baseline values) include: 1. Demographics and past medical history: Age, gender, body mass index (BMI), systolic blood pressure, history and duration of smoking and alcohol consumption and others 2. Chinese medicine diagnosis: presence of Chinese medicine syndromes (e.g. spleen and kidney qi deficiency) based on the presentation of standardised and commonly documented signs and symptoms 3. Biochemical profile

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 118
• Est. completion date: December 31, 2022
• Est. primary completion date: June 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 35 Years to 80 Years

Eligibility

Inclusion Criteria:

• diagnosed with type 2 diabetes for at least 5 years;
• with an estimated glomerular filtration rate (GFR) =30 ?90 mL/min/1.73m2 confirmed with repeat testing over three or more months calculated by the abbreviated MDRD study equation;
• persistent macroalbuminuria with spot urine albumin-to-creatinine ratio (UACR) = 300 mg/g confirmed by at least 2 out of 3 consecutive first morning void urine samples;
• on stable dose of anti-diabetic drug including insulin for 12 weeks;
• on stable dose of angiotensin-converting-enzyme inhibitor or angiotensin receptor blocker for 12 weeks; and
• willing and able to give written informed consent

Exclusion Criteria:

• with known history of glomerulonephritis, polycystic kidney disease, systemic lupus erythematosus, any suggestive evidence of nondiabetic glomerulopathy;
• with known history of kidney transplant;
• with concurrent severe disorders of heart, brain, liver, and hematopoietic system, tumor and mental disorder;
• with deranged liver function;
• poorly controlled blood pressure;
• with known history of intolerance or malabsorption of oral medications;
• with uncontrollable urinary infection;
• experiencing pregnancy; or
• participating in other clinical trial within 30 days

Related Conditions & MeSH terms

• Diabetic Kidney Disease
• Diabetic Nephropathies
• Kidney Diseases

Intervention

Drug:
• Astragalus Powder
3 grams of water soluble astragalus sachets (equivalent to 15g raw herbs) administrated orally on top of standard medical care for 48 weeks. Patients will have 5 days of medicine per week and will be advised to take the medicine once daily dissolved in boiling water in the first 5 days of the week.

Other:
• Routine medical care (active comparator)
Angiotensin converting enzyme inhibitor or angiotensin receptor blocker

Locations

Country	Name	City	State
Hong Kong	Queen Mary Hospital	Hong Kong
Hong Kong	School of Chinese Medicine	Hong Kong

Sponsors (2)

Lead Sponsor	Collaborator
The University of Hong Kong	School of Chinese Medicine, The University of Hong Kong

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Change in biomarkers related to inflammation and fibrosis		From baseline to 48 weeks after treatment
Primary	Change in estimated GFR	Efficacy and safety	From baseline to 48 weeks after treatment
Primary	Change in spot urine albumin-to-creatinine ratio	Efficacy and safety	From baseline to 48 weeks after treatment
Secondary	Change in glycated haemoglobin (HbA1c)		From baseline to 48 weeks after treatment
Secondary	Change in urinary monocyte chemotactic protein 1 (MCP-1)		From baseline to 48 weeks after treatment
Secondary	Change in urinary Cystatin C		From baseline to 48 weeks after treatment
Secondary	Change in lipids		From baseline to 48 weeks after treatment