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 @ 12:39 AM
Ignite Modification Date:
2025-12-25 @ 12:39 AM
NCT ID:
NCT06574867
Eligibility Criteria:
Inclusion Criteria:
* Adult patients (18 years and older).
* Patients admitted to the surgical ward at Catharina Hospital Eindhoven.
* Fluent in Dutch or English.
* Willingness to participate in the study and to wear the viQtor monitoring device during their hospital stay.
Exclusion Criteria:
Patients with cognitive impairments.
* Patients with allergies to metal or plastics.
* Patients with significant deformities, swelling, irritation, degenerative changes, or edema of the upper arm.
* Patients with implanted cardiac pacemakers, internal cardioverter defibrillators, or chronic resynchronization therapy devices.
* Patients at risk of vascular compromise of the arm on which the device will be placed.
* Patients with conditions that contraindicate the use of a blood pressure cuff or similar devices.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06574867
Study Brief:
Protocol Section:
NCT06574867