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 @ 4:58 AM
Ignite Modification Date:
2025-12-25 @ 4:58 AM
NCT ID:
NCT05959018
Eligibility Criteria:
Inclusion Criteria:
* Patients aged 18 years old and above who are admitted to the ICU of UMMC during the study period
* Patients who require a CVC during ICU stay
Exclusion Criteria:
* Patients who refuse to participate in the study
* Patients with known hypersensitivity reaction to CVC materials
* Patients with pre-existing diagnosis of CLABSI upon admission to the ICU
* Patients with pre-existing bloodstream infection upon admission to the ICU
* Patients with a pre-existing CVC, where sterility during placement may be compromised (e.g. in an emergency situation)
* Patients with indwelling CVC less than 48 hours
* Patients who had poor compliance to catheter bundle care during CVC handling throughout the indwelling catheter period
* Patients who require \> 1 CVC or other central venous access
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
100 Years
Study:
NCT05959018
Study Brief:
Protocol Section:
NCT05959018