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The Comparative Effectiveness of Alprostadil,Sodium Ferulate and Dopamine in Pediatric Acute Kidney Injury

Primary Purpose

Children AKI Patients

Status
Unknown status
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Alprostadil
Sodium Ferulate
Dopamine
Sponsored by
Shengjing Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Children AKI Patients focused on measuring AKI, Child, Alprostadil, Sodium Ferulate, Dopamine

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Provide informed consent signed and dated by participants and/or their guardians
  2. male or female, Asian.
  3. Aged from 1 to 18 years.
  4. Patients meet the AKI diagnosis criteria of 2012 Kidney Disease: Improving Global Outcome (SKDIGO) Guideline

Exclusion Criteria:

  1. prerenal or postrenal failure
  2. Patients need renal replacement therapy
  3. Patients with hemorrhagic disorders
  4. Patients in shock
  5. Patients with multiple organ failure
  6. History of Alprostadil or Sodium Ferulate or dopamine sensitivity
  7. Patients with heart failure
  8. Patients with peptic ulcer
  9. Patients with glaucoma
  10. Patients with interstitial pneumonia

Sites / Locations

  • Shenjing Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Alprostadil

Sodium Ferulate

Arm Description

Alprostadil 0.2~0.3ug/kg.h,iv,1h/d,14d; Dopamine3~5 ug/kg·min,iv,3 h/d,14d

Sodium Ferulate 2~6mg/kg.d,iv,14d; Dopamine3~5 ug/kg·min,iv,3 h/d,14d

Outcomes

Primary Outcome Measures

Serum creatinin
The change of Serum creatinin from baseline after the use of the study drug.
eGFR
The change of eGFR from baseline after the use of the study drug. eGFR (ml/min/1.73m2)=K×L/SCr. L: Height(cm), SCr: serum creatinin (umol/L),K:36.5
Urine volume
The change of urine volume from baseline after the use of the study drug.

Secondary Outcome Measures

Urinary markers:White Blood Cell (WBC)
Obtained through routine urine examination.
Urinary markers:Red Blood Cell (RBC)
Obtained through routine urine examination.
Urinary markers:Urine protein
Obtained through routine urine examination.
Serum urea
Obtained through renal function test.
Serum Cystatin
Obtained through renal function test.
Three dimensional(3D) color ultrasound Imaging
Size of kidneys,Blood flow of renal arteries.
Blood pressure
Duration of hospital stays

Full Information

First Posted
March 25, 2019
Last Updated
March 25, 2019
Sponsor
Shengjing Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03892447
Brief Title
The Comparative Effectiveness of Alprostadil,Sodium Ferulate and Dopamine in Pediatric Acute Kidney Injury
Official Title
A 52-week Multicenter, Randomized, Double-blind, Prospective Study to Evaluate Comparative Effectiveness and Safety of Alprostadil Injection,Sodium Ferulate and Dopamine Injection in Pediatric Acute Kidney Injury
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Unknown status
Study Start Date
August 1, 2019 (Anticipated)
Primary Completion Date
April 30, 2021 (Anticipated)
Study Completion Date
December 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shengjing Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Acute kidney injury (AKI) is a pervasive clinical event in children.It has been independently associated with prolonged hospital stays, risk of in-hospital death and future progression to chronic kidney disease. Except for removal of nephrotoxic agents and optimization of supportive care,there are still no other effective therapeutic options recommended by recent guidelines. Renal ischemia is the main mechanism of AKI, the improving microcirculation therapy would be the effective management to improve the outcome of AKI in children. Dopamine is a vasodilating drug that in small doses improves renal circulation. Alprostadil have been used in chronic arterial occlusion and Sodium Ferulate in ischemic cerebral vascular disease,they have a similar therapeutic effect of anti-platelet aggregation and vasodilation. Recent research shows that alprostadil might be associated with a significant reduction in postcontrast Scr, blood urine nitrogen (BUN) and Cystatin C (CysC) level and decrease the incidence of contrast-induced nephropathy.The investigators speculate that Alprostadil,Sodium Ferulate and dopamine would be effective in treating AKI in children. This is a prospective, multicenter, randomized, double-blind, 52-week study. The purpose of this study is to evaluate the comparative effectiveness and safety of Alprostadil,Sodium Ferulate and dopamine in improving the outcome of AKI in children.
Detailed Description
This study aims to explore the effective treatment of pediatric AKI and improve the outcome. It is a 52-week multicenter, randomized, double-blind,prospective study to evaluate comparative effectiveness and safety of alprostadil injection,sodium ferulate and dopamine injection. This study plans to recruit 8 to 10 centers, with 300 participants randomly divided into 3 groups and given respectively Alprostadil 0.2~0.3ug/kg.h,iv,1h/d,14d,Sodium Ferulate2~6mg/kg.d,iv,14d,Dopamine3~5ug/kg .min,iv,3h/d,14d.Time of outcome measurement is 1w,2w,4w,24w,52w. Primary Outcome Measures is The change of Serum creatinin from baseline, estimated glomerular filtration rate (eGFR) and urine volume in the participants after the use of the study drug.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Children AKI Patients
Keywords
AKI, Child, Alprostadil, Sodium Ferulate, Dopamine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
300 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Alprostadil
Arm Type
Experimental
Arm Description
Alprostadil 0.2~0.3ug/kg.h,iv,1h/d,14d; Dopamine3~5 ug/kg·min,iv,3 h/d,14d
Arm Title
Sodium Ferulate
Arm Type
Active Comparator
Arm Description
Sodium Ferulate 2~6mg/kg.d,iv,14d; Dopamine3~5 ug/kg·min,iv,3 h/d,14d
Intervention Type
Drug
Intervention Name(s)
Alprostadil
Intervention Description
Alprostadil 0.2~0.3ug/kg.h,iv,1h/d,14d
Intervention Type
Drug
Intervention Name(s)
Sodium Ferulate
Intervention Description
Sodium Ferulate 2~6mg/kg.d,iv,14d
Intervention Type
Drug
Intervention Name(s)
Dopamine
Intervention Description
Dopamine3~5 ug/kg·min,iv,3 h/d,14d
Primary Outcome Measure Information:
Title
Serum creatinin
Description
The change of Serum creatinin from baseline after the use of the study drug.
Time Frame
baseline, 52 weeks
Title
eGFR
Description
The change of eGFR from baseline after the use of the study drug. eGFR (ml/min/1.73m2)=K×L/SCr. L: Height(cm), SCr: serum creatinin (umol/L),K:36.5
Time Frame
baseline, 52 weeks
Title
Urine volume
Description
The change of urine volume from baseline after the use of the study drug.
Time Frame
baseline, 52 weeks
Secondary Outcome Measure Information:
Title
Urinary markers:White Blood Cell (WBC)
Description
Obtained through routine urine examination.
Time Frame
baseline, 52 weeks
Title
Urinary markers:Red Blood Cell (RBC)
Description
Obtained through routine urine examination.
Time Frame
baseline, 52 weeks
Title
Urinary markers:Urine protein
Description
Obtained through routine urine examination.
Time Frame
baseline, 52 weeks
Title
Serum urea
Description
Obtained through renal function test.
Time Frame
baseline, 52 weeks
Title
Serum Cystatin
Description
Obtained through renal function test.
Time Frame
baseline, 52 weeks
Title
Three dimensional(3D) color ultrasound Imaging
Description
Size of kidneys,Blood flow of renal arteries.
Time Frame
baseline, 52 weeks
Title
Blood pressure
Time Frame
baseline, 52 weeks
Title
Duration of hospital stays
Time Frame
baseline, 52 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Provide informed consent signed and dated by participants and/or their guardians male or female, Asian. Aged from 1 to 18 years. Patients meet the AKI diagnosis criteria of 2012 Kidney Disease: Improving Global Outcome (SKDIGO) Guideline Exclusion Criteria: prerenal or postrenal failure Patients need renal replacement therapy Patients with hemorrhagic disorders Patients in shock Patients with multiple organ failure History of Alprostadil or Sodium Ferulate or dopamine sensitivity Patients with heart failure Patients with peptic ulcer Patients with glaucoma Patients with interstitial pneumonia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yubin Wu, Professor
Phone
18940257958
Email
wuyb001@163.com
Facility Information:
Facility Name
Shenjing Hospital
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110004
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Dear Sir/Madam Our study receives a grant from China Ministry of Science and Technology. We cannot decide whether the data could be shared. Hope you can understand.
Links:
URL
http://kdigo.org/
Description
2012 SKDIGO Guideline

Learn more about this trial

The Comparative Effectiveness of Alprostadil,Sodium Ferulate and Dopamine in Pediatric Acute Kidney Injury

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