NCT06012994

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
160

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2018

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2018

Completed
2.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2021

Completed
2.1 years until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2023

Completed
20 days until next milestone

First Submitted

Initial submission to the registry

August 20, 2023

Completed
8 days until next milestone

First Posted

Study publicly available on registry

August 28, 2023

Completed
Last Updated

August 28, 2023

Status Verified

August 1, 2023

Enrollment Period

2.6 years

First QC Date

August 20, 2023

Last Update Submit

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

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Location

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

Locations