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Routine and Deferred Dialysis Initiation (RADDI)

Primary Purpose

Chronic Kidney Disease

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Algorithm for deferred dialysis intervention
Algorithm for routine dialysis intervention
Sponsored by
Peking University People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Disease

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Nondialysis-dependent stable CKD stage 4-5 patients (eGFR>7ml/min /1.73 m2)
  2. Willing to choose dialysis as his renal replacement therapy method
  3. Heart function: grade I or II (NYHA Functional Classification)

Exclusion Criteria:

  1. The life expectancy of patients is estimated to be short (due to causes other than kidney disease);
  2. Acute infection occurred in one month;
  3. Myocardial infarction, NYHA class IV or stroke events within 3 months;
  4. Uncontrolled malignancy;
  5. Active viral hepatitis;
  6. Active rheumatic disease;
  7. Pregnant women, women intending to conceive after enrollment or breastfeeding woman;
  8. Planning to take kidney transplantation within the study period;
  9. With indices of emergency dialysis;
  10. eGFR less than 7 ml/min/1.73m2 in first visit;
  11. Under other clinical studies which has an impact on this study;
  12. Unable to provide written informed consent.

Sites / Locations

  • Peking University People's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Deffered Dialysis Initiation

Routine dialysis Initiation

Arm Description

Algorithm for deferred dialysis intervention: initiating dialysis in the absence of symptoms in patients with an eGFR of 5 ml/min /1.73 m2 or less

Algorithm for routine dialysis intervention: initiating dialysis in the absence of symptoms in patients with an eGFR of 7 ml/min /1.73 m2 (which is the average GFR for patients in Beijing to start dialysis )

Outcomes

Primary Outcome Measures

All-cause mortality: Proportion of patients who die from any cause
Proportion of patients who die from any cause during observation period.
Acute nonfatal cerebro-cardiovascular events before dialysis initiation
Proportion of patients who suffer from acute nonfatal cerebro-cardiovascular events before dialysis initiation. Cerebro-cardiovascular events include acute myocardial infarction,acute coronary ischemia syndrome,acute heart failure, acute exacerbation of chronic heart failure ,severe arrhythmia, stroke, etc.
Acute nonfatal cerebro-cardiovascular events after dialysis initiation
Proportion of patients who suffer from acute nonfatal cerebro-cardiovascular events after dialysis initiation. Cerebro-cardiovascular events include acute myocardial infarction,acute coronary ischemia syndrome,acute heart failure, acute exacerbation of chronic heart failure ,severe arrhythmia, stroke, etc.

Secondary Outcome Measures

Hospitalization: Proportion of patients who are admitted to hospital
Proportion of patients who are admitted to hospital
Nutrition assessment
SGA assessment and serum albumin level are used to assess nutrition status
Patient reported outcome of quality of life
The short form health survey questionnaire 36 will be used.
Complications of dialysis
Proportion of patients who suffer from dialysis complications including blood acess infection, thrombosis, hypotension, etc.
Costs
All money patients and insurance agency spend on medical care related with CKD
Arteriovenous fistulas usage
Proportion of patients using arteriovenous fistulas as their blood access when dialysis initiation. The timing for preparing arteriovenous fistulas depends on the past GFR decline trajectory
Catheter usage
Proportion of patients using catheter as their blood access when dialysis initiation.

Full Information

First Posted
April 10, 2015
Last Updated
April 11, 2019
Sponsor
Peking University People's Hospital
Collaborators
Peking University First Hospital, Sichuan Academy of Medical Sciences, First Affiliated Hospital of Zhejiang University, The First Affiliated Hospital of Zhengzhou University, Shaanxi Hospital of Traditional Chinese Medicine, Peking Union Medical College Hospital, Shengjing Hospital, The First Affiliated Hospital of BaoTou Medical College, Beijing Hospital, National Center of Gerontology, Beijing Haidian Hospital/Beijing Haidian Section of Peking University Third Hospital, Beijing Tongren Hospital, Xuanwu Hospital, Beijing, First Hospital of China Medical University, Hangzhou Hospital of Traditional Chinese Medicine, Ruijin Hospital Affiliated to Shanghai Jiao Tong University
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1. Study Identification

Unique Protocol Identification Number
NCT02423655
Brief Title
Routine and Deferred Dialysis Initiation
Acronym
RADDI
Official Title
A Randomized, Controlled Trial to Evaluate Routine and Deferred Dialysis Initiation in Chinese Population
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Unknown status
Study Start Date
July 2015 (Actual)
Primary Completion Date
August 2020 (Anticipated)
Study Completion Date
December 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Peking University People's Hospital
Collaborators
Peking University First Hospital, Sichuan Academy of Medical Sciences, First Affiliated Hospital of Zhejiang University, The First Affiliated Hospital of Zhengzhou University, Shaanxi Hospital of Traditional Chinese Medicine, Peking Union Medical College Hospital, Shengjing Hospital, The First Affiliated Hospital of BaoTou Medical College, Beijing Hospital, National Center of Gerontology, Beijing Haidian Hospital/Beijing Haidian Section of Peking University Third Hospital, Beijing Tongren Hospital, Xuanwu Hospital, Beijing, First Hospital of China Medical University, Hangzhou Hospital of Traditional Chinese Medicine, Ruijin Hospital Affiliated to Shanghai Jiao Tong University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the efficacy and safety of deferred dialysis initiation in Chinese population. 16 tertiary hospitals across China will be randomly assigned into routine and deferred dialysis groups.
Detailed Description
The timing for initiating dialysis for progressive chronic kidney disease (CKD) patients is an important issue yet is not well established. There is a strong trend to early dialysis initiation for end stage renal disease (ESRD) patients over the past decades. However, observational data found that early initiation seemed to produce no benefit but additional burden to patients and the health care system. The IDEAL study, the only randomized, controlled trial (RCT) on this issue, found that all-cause mortality, comorbidities and quality of life had no difference between early (glomerular filtration rate, GFR 10-14ml/min/1.73m2) and late (GFR 5-7ml/min/1.73m2) dialysis starters. However there was a big limitation in this study that the difference for average GFR between two groups (12 ml/min/1.73 m2 vs. 9.8 ml/min/1.73m2) was not so separate. Recently, the Canadian Society of Nephrology have released a clinical practice guideline on this issue. The guideline recommends an "intent-to-defer" approach for dialysis initiation and to initiate dialysis in the absence of symptoms in patients with an estimated GFR of 6 ml/min /1.73 m2 or less. In this guideline the specialists also express that the optimal management of patients with an estimated GFR of 6 ml/min per 1.73 m2 or less is based on limited data. There is a gap in knowledge. This research will further evaluate the efficacy and safety of deferred dialysis initiation and fill in this gap. In this study, algorithms will be adopted to determine the timing of dialysis initiation for both routine and deferred dialiysis groups, and the only difference in these two algorithms is the GFR level to initiate dialysis (7 Vs. <5 ml/min per 1.73 m2). The theory that blood access (arteriovenous fistulas) can be timely prepared according to the past GFR decline trajectory will also be tested.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1049 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Deffered Dialysis Initiation
Arm Type
Experimental
Arm Description
Algorithm for deferred dialysis intervention: initiating dialysis in the absence of symptoms in patients with an eGFR of 5 ml/min /1.73 m2 or less
Arm Title
Routine dialysis Initiation
Arm Type
Active Comparator
Arm Description
Algorithm for routine dialysis intervention: initiating dialysis in the absence of symptoms in patients with an eGFR of 7 ml/min /1.73 m2 (which is the average GFR for patients in Beijing to start dialysis )
Intervention Type
Other
Intervention Name(s)
Algorithm for deferred dialysis intervention
Intervention Description
Use combined indications to guide researchers to defer dialyzing progressive CKD patients. Asymptomatic patient will not start dialysis treatment until his eGFR becomes less than 5 ml/min/1.73m2. Or until 1. Patient's Kraemer index is >6 or with overt fluid overload after trying all conservative means(including appropriate medicines) 2. Patient's Subjective Global Assessment method (SGA) assessment is grade C 3. Patients have indications for emergency dialysis 4. Sever symptoms which cannot be relieved by conservative treatment
Intervention Type
Other
Intervention Name(s)
Algorithm for routine dialysis intervention
Intervention Description
Use combined indications to guide researchers to initiate dialysis in progressive CKD patients routinely. Researchers will start dialysis treatment for a patient when his eGFR reaches 7 ml/min/1.73m2 in asymptomatic patients. Or patients have indications below: 1. Patient's Kraemer index is >6 or with overt fluid overload after trying all conservative means(including appropriate medicines) 2. Patient's SGA assessment is grade C 3. Patients have indications for emergency dialysis 4. Sever symptoms which cannot be relieved by conservative treatment
Primary Outcome Measure Information:
Title
All-cause mortality: Proportion of patients who die from any cause
Description
Proportion of patients who die from any cause during observation period.
Time Frame
From date of enrollment until the end of study, assessed up to 3 years
Title
Acute nonfatal cerebro-cardiovascular events before dialysis initiation
Description
Proportion of patients who suffer from acute nonfatal cerebro-cardiovascular events before dialysis initiation. Cerebro-cardiovascular events include acute myocardial infarction,acute coronary ischemia syndrome,acute heart failure, acute exacerbation of chronic heart failure ,severe arrhythmia, stroke, etc.
Time Frame
From date of enrollment until the date of dialysis initiation, or the date of death from any cause,or the end of study, whichever came first, assessed up to 3 year
Title
Acute nonfatal cerebro-cardiovascular events after dialysis initiation
Description
Proportion of patients who suffer from acute nonfatal cerebro-cardiovascular events after dialysis initiation. Cerebro-cardiovascular events include acute myocardial infarction,acute coronary ischemia syndrome,acute heart failure, acute exacerbation of chronic heart failure ,severe arrhythmia, stroke, etc.
Time Frame
From date of dialysis initiation until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 year
Secondary Outcome Measure Information:
Title
Hospitalization: Proportion of patients who are admitted to hospital
Description
Proportion of patients who are admitted to hospital
Time Frame
From date of enrollment until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 year
Title
Nutrition assessment
Description
SGA assessment and serum albumin level are used to assess nutrition status
Time Frame
From date of enrollment until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 years, performed every 3 months
Title
Patient reported outcome of quality of life
Description
The short form health survey questionnaire 36 will be used.
Time Frame
From date of enrollment until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 years, once every 3 months
Title
Complications of dialysis
Description
Proportion of patients who suffer from dialysis complications including blood acess infection, thrombosis, hypotension, etc.
Time Frame
From date of dialysis initiation until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 year
Title
Costs
Description
All money patients and insurance agency spend on medical care related with CKD
Time Frame
From date of enrollment until the date of death from any cause,or the end of study, whichever came first, assessed up to 3 years, performed every 3 months
Title
Arteriovenous fistulas usage
Description
Proportion of patients using arteriovenous fistulas as their blood access when dialysis initiation. The timing for preparing arteriovenous fistulas depends on the past GFR decline trajectory
Time Frame
From date of enrollment until the date of dialysis initiation, assessed up to 3 years
Title
Catheter usage
Description
Proportion of patients using catheter as their blood access when dialysis initiation.
Time Frame
From date of enrollment until the date of dialysis initiation, assessed up to 3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Nondialysis-dependent stable CKD stage 4-5 patients (eGFR>7ml/min /1.73 m2) Willing to choose dialysis as his renal replacement therapy method Heart function: grade I or II (NYHA Functional Classification) Exclusion Criteria: The life expectancy of patients is estimated to be short (due to causes other than kidney disease); Acute infection occurred in one month; Myocardial infarction, NYHA class IV or stroke events within 3 months; Uncontrolled malignancy; Active viral hepatitis; Active rheumatic disease; Pregnant women, women intending to conceive after enrollment or breastfeeding woman; Planning to take kidney transplantation within the study period; With indices of emergency dialysis; eGFR less than 7 ml/min/1.73m2 in first visit; Under other clinical studies which has an impact on this study; Unable to provide written informed consent.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Li Zuo
Organizational Affiliation
Peking University People's Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Peking University People's Hospital
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100044
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
24066675
Citation
Rosansky SJ, Cancarini G, Clark WF, Eggers P, Germaine M, Glassock R, Goldfarb DS, Harris D, Hwang SJ, Imperial EB, Johansen KL, Kalantar-Zadeh K, Moist LM, Rayner B, Steiner R, Zuo L. Dialysis initiation: what's the rush? Semin Dial. 2013 Nov-Dec;26(6):650-7. doi: 10.1111/sdi.12134. Epub 2013 Sep 19.
Results Reference
result
PubMed Identifier
20581422
Citation
Cooper BA, Branley P, Bulfone L, Collins JF, Craig JC, Fraenkel MB, Harris A, Johnson DW, Kesselhut J, Li JJ, Luxton G, Pilmore A, Tiller DJ, Harris DC, Pollock CA; IDEAL Study. A randomized, controlled trial of early versus late initiation of dialysis. N Engl J Med. 2010 Aug 12;363(7):609-19. doi: 10.1056/NEJMoa1000552. Epub 2010 Jun 27.
Results Reference
result
PubMed Identifier
24508475
Citation
Crews DC, Scialla JJ, Boulware LE, Navaneethan SD, Nally JV Jr, Liu X, Arrigain S, Schold JD, Ephraim PL, Jolly SE, Sozio SM, Michels WM, Miskulin DC, Tangri N, Shafi T, Wu AW, Bandeen-Roche K; DEcIDE Network Patient Outcomes in End Stage Renal Disease Study Investigators. Comparative effectiveness of early versus conventional timing of dialysis initiation in advanced CKD. Am J Kidney Dis. 2014 May;63(5):806-15. doi: 10.1053/j.ajkd.2013.12.010. Epub 2014 Feb 6.
Results Reference
result
PubMed Identifier
24492525
Citation
Nesrallah GE, Mustafa RA, Clark WF, Bass A, Barnieh L, Hemmelgarn BR, Klarenbach S, Quinn RR, Hiremath S, Ravani P, Sood MM, Moist LM; Canadian Society of Nephrology. Canadian Society of Nephrology 2014 clinical practice guideline for timing the initiation of chronic dialysis. CMAJ. 2014 Feb 4;186(2):112-7. doi: 10.1503/cmaj.130363. No abstract available.
Results Reference
result
PubMed Identifier
31818266
Citation
Zhao X, Wang P, Wang L, Chen X, Huang W, Mao Y, Hu R, Cheng X, Wang C, Wang L, Zhang P, Li D, Wang Y, Ye W, Chen Y, Jia Q, Yan X, Zuo L. Protocol for a prospective, cluster randomized trial to evaluate routine and deferred dialysis initiation (RADDI) in Chinese population. BMC Nephrol. 2019 Dec 9;20(1):455. doi: 10.1186/s12882-019-1627-0.
Results Reference
derived
Links:
URL
http://www.phbjmu.edu.cn/
Description
The website of Peking University People's Hospital

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Routine and Deferred Dialysis Initiation

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