- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04466306
Pediatric Acute Kidney Injury in COVID-19 (SPARC-1)
SARS-CoV2 Pediatric Acute Kidney Injury Registry and Collaborative
Study Overview
Status
Conditions
Detailed Description
The primary purpose of the data collection will be to provide a descriptive analysis of the burden and characteristics of AKI in children with SARS-CoV2 proven or suspected infection across the world. This is a prospective, point prevalence study. Data collection will occur once a week during the months of April through June 2020.
The protocol for the point prevalence is for each individual participating site to conduct a surveillance study on predetermined dates of their intensive care units (pediatric medical, surgical, cardiac ICUs) for patients by the inclusion and exclusion criteria. The study is strictly observational. Data will only be captured on the predetermined dates listed. The dates have been chosen to reflect the estimated surge and peak of the virus spread in North America, Europe, Africa, Asia, and Australia. The rationale for performing an urgent point prevalence estimation study first, includes the following: a) there is almost no knowledge on AKI rate, severity of AKI or how current pandemic-setting AKI phenotype differs from what we know of AKI in children prior to the pandemic. A rapidly-performed, high feasibility-designed point prevalence estimation study, with minimal data collection will provide rapid, almost instantaneous dissemination of results to the international community. Based on the results of this study, a follow-up study is planned for a full retrospective data collection of all viral positive patients. Understanding the burden of pediatric AKI during this pandemic within the current context of acute health burden in the healthcare settings and enable planning and feasibility evaluation for quality of care measures and potentially for upcoming technology needs and/or sharing of RRT technology with adult care units; b) an urgent point-prevalence estimation study with minimal but key data collection will inform on any changes to design, sample size requirements or data points for the larger granular longitudinal retrospective study.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Alberta
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Edmonton, Alberta, Canada, T6G 2C8
- Stollery Children's Hospital
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Ontario
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Hamilton, Ontario, Canada, L8N 3Z5
- McMaster Children's Hospital
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Toronto, Ontario, Canada, M5G 1X8
- The Hospital for Sick Children (SickKids)
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Be'er Sheva, Israel
- Soroka university medical center
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Tel Aviv, Israel
- Dana-Dwek Children's Hospital
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Shizuoka, Japan
- Shizuoka Children's Hospital
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Belgrade, Serbia
- Institute for Mother and Child Healthcare
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Belgrade, Serbia
- University Children's Hospital
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Madrid, Spain
- Hospital 12 de Octubre
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Birmingham, United Kingdom, B4 6NH
- Birmingham Children's Hospital NHS
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Liverpool, United Kingdom
- Alder Hey Children's Hospital NHS
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London, United Kingdom, SE5 9RS
- King's College Hospital NHS
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London, United Kingdom, SW17 0QT
- St. George's University Hospital NHS
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London, United Kingdom, WC1N 3JH
- Great Ormond Street Hospital NHS
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Alabama
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Birmingham, Alabama, United States, 35233
- Children's Hospital of Alabama
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Arkansas
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Little Rock, Arkansas, United States, 72202
- Arkansas Children's Research Institute
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California
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Los Angeles, California, United States, 90095
- UCLA Mattel Children's Hospital
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Los Angeles, California, United States, 90048
- Cedars-Sinai Maxine Dunitz Children's Health Center
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Palo Alto, California, United States, 94304
- Lucile Packard Children's Hospital Standford
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San Diego, California, United States, 92123
- Rady Children's Hospital San Diego
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Colorado
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Aurora, Colorado, United States, 80045
- Children's Hospital Colorado
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Connecticut
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New Haven, Connecticut, United States, 06504
- Yale New Haven Children's Hospital
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Florida
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Gainesville, Florida, United States, 32608
- UF Health Shands Children's Hospital
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Georgia
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Atlanta, Georgia, United States, 30322
- Children's Healthcare of Atlanta
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Illinois
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Chicago, Illinois, United States, 60637
- Comer Children's Hospital - UChicago Medicine
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Indiana
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Indianapolis, Indiana, United States, 46202
- Riley Hospital for Children
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Iowa
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Iowa City, Iowa, United States, 52242
- University of Iowa Stead Family Children's Hospital
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Kansas
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Kansas City, Kansas, United States, 64108
- Children's Mercy
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Maryland
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Baltimore, Maryland, United States, 21287
- John Hopkins Children's Center
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Massachusetts
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Boston, Massachusetts, United States, 02115
- Boston Children's Hospital
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Michigan
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Ann Arbor, Michigan, United States, 48109
- C.S. Mott Children's Hospital
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Grand Rapids, Michigan, United States, 49503
- Helen DeVos Children's Hospital
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Royal Oak, Michigan, United States, 48073
- Beaumont Children's Hospital
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Missouri
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Saint Louis, Missouri, United States, 63110
- St. Louis Children's Hospital of Washington University
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New York
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Buffalo, New York, United States, 14203
- Oishei Children's Hospital of Buffalo
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Rochester, New York, United States, 14642
- Golisano Children's Hospital - University of Rochester Medicine
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Stony Brook, New York, United States, 11794
- Stony Brook Children's Hospital
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North Carolina
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Charlotte, North Carolina, United States, 28203
- Levine Children's Hospital
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Durham, North Carolina, United States, 27705
- Duke Children's Hospital and Health Center
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Ohio
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Cincinnati, Ohio, United States, 45229
- Cincinnati Children's Hospital Medical Center
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Columbus, Ohio, United States, 43205
- Nationwide Children's Hospital
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Pennsylvania
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Hershey, Pennsylvania, United States, 17033
- Penn State Children's Hospital
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Philadelphia, Pennsylvania, United States, 19104
- Children's Hospital of Philadelphia
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Pittsburgh, Pennsylvania, United States, 15224
- UPMC Children's Hospital of Pittsburgh
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Rhode Island
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Providence, Rhode Island, United States, 02903
- Lifespan Hasbro Children's Hospital
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South Carolina
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Charleston, South Carolina, United States, 29425
- Medical University of South Carolina Shawn Jenkins Children's Hospital
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Washington
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Seattle, Washington, United States, 98105
- Seattle Children's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient less than or equal to 25 years of age
- Receiving clinical care in the pediatric intensive care unit (PICU) on a study day in April - June 2020
- Patient considered a "Person Under Investigation" and/or tested positive for SARS-CoV2 (COVID-19)
Exclusion Criteria:
• None
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Acute Kidney Injury (AKI)
Time Frame: 14 days
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Kidney Disease Improving Global Outcomes (KDIGO) Staged AKI by serum creatinine or urine output
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14 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Survival
Time Frame: 14 days
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Survival to ICU discharge or Day 14
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14 days
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Rate of Extracorporeal Therapy Requirement
Time Frame: 14 days
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The use of extracorporeal membrane oxygenation (ECMO) and/or renal replacement therapy
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14 days
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Fluid overload
Time Frame: Day of Enrollment
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>20% fluid overload as defined as the net fluid balance since ICU admission (in liters) divided by ICU admission weight
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Day of Enrollment
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Rate of nephrotoxic medication exposure
Time Frame: Day of Enrollment
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The exposure of enrolled patients to known nephrotoxic medications, including diuretics
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Day of Enrollment
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Rajit K Basu, MD, Children's Healthcare of Atlanta
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ChildrensHA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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