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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ChiCTR |
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Last refreshed on:
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18 April 2017 |
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Main ID: |
ChiCTR-IPR-16007909 |
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Date of registration:
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2016-02-07 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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Clinical Trial of West-China Transfusion Score for Children
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Scientific title:
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Safty and effectiveness of Pediatric Peri-Operative Transfusion Trigger Score: A Multi-Center, Randomized and Controled Research |
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Date of first enrolment:
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2016-03-01 |
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Target sample size:
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control group:500;experimental group:500; |
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Recruitment status: |
Pending |
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URL:
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http://www.chictr.org.cn/showproj.aspx?proj=13361 |
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Study type:
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Interventional study |
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Study design:
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Randomized parallel controlled trial
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Phase:
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Pilot study
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Countries of recruitment
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China
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Contacts
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Name:
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Zhen Luo/Yansong Li
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Address:
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37 Guoxuexiang, Chengdu, China
610041
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Telephone:
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+86 18980602212/13541234031 |
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Email:
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liyansong.inter@163.com |
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Affiliation:
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Department of Anesthesiology, West China Hospital |
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Name:
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Yunxia Zuo
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Address:
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37 Guoxuexiang, Chengdu, China
610041
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Telephone:
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+86 18980601541 |
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Email:
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769574913@qq.com |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion criteria: Less than 14;Resident at an altitude of less than 2500 meters; During peri-operation, hemoglobin level may less than 10g/dL for children between 7-14 years; 11g/dL for children between 1-7 years; 12g/dL for children between 1 month -1 years; 13g/dL for neonate
Exclusion criteria: Emergency operation; Reoperation; Transplant operation; Premature and low birth weight infants (less than 2500g); Serious blood system diseases; Tumor metastasis; Psychopathy or paralysis; join in other research
Age minimum:
0
Age maximum:
14
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Disease which need transfusion
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Intervention(s)
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control group:Transfusion trigger at 10g/dL for neonate 8g/dL for other children, target based on the experience of the doctor;experimental group:transfusion trigger based on West-China Transfusion Score;
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Primary Outcome(s)
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rate of severe complication;
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Secondary Outcome(s)
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Length of ICU stay;Hemoglobin level postoperatively;Length of hospitalization;Cost of transfusion and hospitalization;Quality of life;
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Source(s) of Monetary Support
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West China Hospital
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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