Retrospective Study of the Protective Effect of Gastrodin on Myocardium in Patients Undergoing Cardiac Surgery
1 other identifier
observational
160
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Dec 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 30, 2021
CompletedStudy Completion
Last participant's last visit for all outcomes
July 31, 2023
CompletedFirst Submitted
Initial submission to the registry
August 20, 2023
CompletedFirst Posted
Study publicly available on registry
August 28, 2023
CompletedAugust 28, 2023
August 1, 2023
2.6 years
August 20, 2023
August 25, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
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
Study Arms (2)
GAS
Control
Eligibility Criteria
This study included patients who were preoperatively diagnosed as requiring elective thoracic cardiac surgery under general anesthesia.
You may qualify if:
- Patients aged≥18 years, regardless of gender;
- Patients undergoing elective cardiac surgery under general anesthesia;
- ASA grade 1 \~ 3.
You may not qualify if:
- 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)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
Wuhan, Hubei, 430022, China
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
August 20, 2023
First Posted
August 28, 2023
Study Start
December 1, 2018
Primary Completion
June 30, 2021
Study Completion
July 31, 2023
Last Updated
August 28, 2023
Record last verified: 2023-08