Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 1:22 AM
Ignite Modification Date:
2025-12-25 @ 1:22 AM
NCT ID:
NCT06508593
Eligibility Criteria:
Inclusion Criteria:
1. 18 years old and above
2. Patients undergone elective cardiac surgery
3. History of serum creatinine test within 7 days before surgery
4. Provide venous blood samples
5. Voluntarily participate and sign an informed consent form
Exclusion Criteria:
1. Patients treated with chronic peritoneum or hemodialysis, prior kidney transplantation, preoperative serum creatinine level\>4.5mg/dL (400 μ mol/L) or end-stage renal disease (defined as glomerular filtration rate\<15ml · min-1 · 1.73m-2)
2. Other related diseases that have been previously confirmed to have cognitive impairment, or records of using drugs targeting cognitive impairment during the onset period
3. Individuals with severe speech, visual, hearing, or mental impairments that affect cognitive scale assessment
4. Individuals with a history of brain tumors, traumatic brain injury, brain parasitic diseases, and other diseases that may cause cognitive impairment
5. Individuals with a history of alcohol and drug addiction
6. Pregnant and lactating women
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06508593
Study Brief:
Protocol Section:
NCT06508593