Ignite Creation Date:
2024-05-06 @ 8:26 PM
Last Modification Date:
2024-10-26 @ 3:27 PM
Study NCT ID:
NCT06383208
Status:
RECRUITING
Last Update Posted:
2024-04-25
First Post:
2024-04-21
Brief Title:
Cardiovascular-Renal Adverse Prognosis Assessment System for Coronary Heart Disease With Chronic Kidney Disease Based on Metabolomics
Sponsor:
Organization:
China-Japan Friendship Hospital
Study Design
Study Type:
OBSERVATIONAL
Expanded Access Type Individual:
None
Expanded Access Type Intermediate:
None
Expanded Access Type Treatment:
None
Patient Registry:
True
Target Duration:
12 Months
Design Allocation:
Design Intervention Model:
Design Intervention Model Description:
Design Masking Description:
Bio Spec Retention:
SAMPLES_WITHOUT_DNA
Bio Spec Description:
Collect 4 ml of fasting peripheral venous blood from enrolled patients Fasting should commence at 2200 the day before blood collection The blood should be placed in EDTA anticoagulant tubes
Within 2 hours after blood collection plasma should be separated and stored for subsequent lipidomic analysis This involves centrifuging at 3000 rpm for 10 minutes to separate the plasma Transfer the upper layer of plasma into 200 ul15 ml EP tubes then store at -80C for preservation
Enrollment Count:
470
Enrollment Type:
ESTIMATED
Design Primary Purpose:
Design Masking:
Phases:
Observational Models:
| Name |
|---|
| Cohort |
Time Perspective List:
Clinical Trial Statuses
| Name |
|---|
| 106333 |
Who Masked List: