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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04980742
Other study ID # 2017-111
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 1, 2017
Est. completion date December 31, 2021

Study information

Verified date August 2020
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Min Yan, doctor
Phone +86-571-87783716
Email zryanmin@zju.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Based on a review of about 10,000 patients undergoing cardiac surgery under CPB in West China Hospital of Sichuan University and the Second Affiliated Hospital of Zhejiang University, we try to evalute the effect of blood transfusion on outcomes in cardiac surgery.


Description:

Based on a review of about 10,000 patients undergoing cardiac surgery under CPB in West China Hospital of Sichuan University and the Second Affiliated Hospital of Zhejiang University, the following results were obtained: 1. Perioperative risk factors of death and complications of different organ systems after cardiac surgery, providing evidence for early prevention and intervention; 2. Risk factors of blood transfusion risk were analyzed to provide ideas for reducing intraoperative blood transfusion; 3. The relationship between hemoglobin and complications after heart surgery was explored to provide a factual basis for the development of blood transfusion indications for such patients


Recruitment information / eligibility

Status Recruiting
Enrollment 3000
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - The patients in the west China hospital of sichuan university (July 01, 2011, solstice during June 30, 2017) and the second affiliated hospital of zhejiang university (September 01, 2013, solstice, June 30, 2017) have cardiac surgery under Cardiopulmonary bypass (CPB) Exclusion Criteria: - No

Study Design


Intervention

Procedure:
acute normovolemic hemodilution
acute normovolemic hemodilution

Locations

Country Name City State
China ANH Hangzhou

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary mortality all-cause death 28 days after surgery
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