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 @ 12:36 AM
Ignite Modification Date:
2025-12-25 @ 12:36 AM
NCT ID:
NCT01565967
Eligibility Criteria:
Inclusion Criteria:
* Patients with an indication for surgery procedures in which the hospital treatment protocol requires the routine use of an autotransfusion system are eligible for participation.
Exclusion Criteria:
* The use of citrate-based anticoagulant in patients with impaired liver function
* Gross contamination and/or septic procedures
* Surgery within the malignant area that may allow dissemination of tumor/malignant cells, if aspirated, into the autotransfusion system
* Caesarean sections in presence of amniotic fluid
* Presence of high concentrations of prostatic fluid
* Contamination of salvaged blood with drugs not intended for intravenous administration
* Use of collagen-based haemostatic agents and gel foam used in combination with any autotransfusion system
* Coagulopathy
* Not willing to sign a Patient Informed Consent/Data Release Form
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT01565967
Study Brief:
Protocol Section:
NCT01565967