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:
2026-03-26 @ 3:19 PM
Ignite Modification Date:
2026-03-26 @ 3:19 PM
NCT ID:
NCT07329660
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years;
* Patients scheduled to undergo elective TAVR under general anesthesia;
Exclusion Criteria:
* Allergy to hydroxyethyl starch, its components, and/or sodium lactate Ringer's solution, or a history of colloidal allergy;
* Severe cardiac dysfunction (ejection fraction\[EF\] \< 35%);
* Severe renal dysfunction (creatinine \> 132 μg/L and/or requiring renal replacement therapy);
* Morbid obesity (body mass index\[BMI\] \> 37.5 kg/m² or \> 32.5 kg/m² with metabolic diseases);
* Severe hepatic dysfunction ;
* Severe electrolyte disturbances ;
* Patients with preoperative intracranial hypertension requiring dehydration therapy;
* Expected postoperative hospital stay \< 24 hours;
* Patients scheduled for multiple surgeries during this hospitalization.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07329660
Study Brief:
Protocol Section:
NCT07329660