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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06012994
Other study ID # mzk202303
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 1, 2018
Est. completion date July 31, 2023

Study information

Verified date August 2023
Source Wuhan Union Hospital, China
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Retrospective collection of Wuhan Union hospital from December 1,2018 to June 30,2021 to meet the entry and discharge standards. The patient 's medical record data were divided into study group and control group according to the use of gastrodin during operation. The perioperative data and prognostic outcomes in the patient 's medical records were collected and analyzed. The degree of myocardial injury and postoperative clinical outcomes were compared between the two groups.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date July 31, 2023
Est. primary completion date June 30, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients aged=18 years, regardless of gender; - Patients undergoing elective cardiac surgery under general anesthesia; - ASA grade 1 ~ 3. Exclusion Criteria: - Suffering from more serious genetic diseases (such as immunodeficiency, thalassemia, etc.); - Moderate to severe malnutrition, moderate to severe anemia; - Persistent infection; - Severe preoperative underlying diseases (such as severe liver and kidney dysfunction)

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
China Union Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan Hubei

Sponsors (1)

Lead Sponsor Collaborator
Wuhan Union Hospital, China

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary The degree of myocardial injury The myocardial tissue trimmed by the surgeon according to the surgical requirements was collected during the operation for electron microscopy observation and detection of related molecular content. The myocardial tissue was collected during the operation. About 2 hours on average
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