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 @ 12:58 AM
Ignite Modification Date:
2025-12-25 @ 12:58 AM
NCT ID:
NCT04918693
Eligibility Criteria:
Participant Inclusion criteria
1. Completed advanced training (e.g., fellowship) in or hold a qualification related to UGRA
2. Regularly delivers direct clinical care using UGRA, including for 'awake' surgery where indicated
3. Member of a relevant professional society (e.g., ASA, ASRA, ESRA, RA-UK)
4. Regularly teach UGRA in the course of their clinical work, including advanced techniques where indicated
Participant exclusion criteria
1. Unwilling or unable to provide informed consent.
2. Involved in development of the ScanNav Anatomy PNB device.
Trainee Inclusion criteria
1. U.S. board-eligible/board-certified health practitioner who holds a qualification licensing to perform UGRA
2. NOT capable or confident of independent UGRA practice
Trainee exclusion criteria
1. Unwilling or unable to provide informed consent.
2. Involved in development of the ScanNav Anatomy PNB device.
Models Inclusion Criteria
1. Male or female, at least 18 years of age;
2. Able to comprehend and sign the Informed Consent prior to enrolment in the study.
3. To fit either BMI category: BMI \<30 OR BMI \>=30
Model Exclusion Criteria
1. Aged \<18 years of age or over 60 years or age
2. Unwilling or unable to provide informed consent.
3. BMI\> 39 kg/m2
4. Known pathology of the area to be scanned.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
70 Years
Study:
NCT04918693
Study Brief:
Protocol Section:
NCT04918693