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 @ 3:20 AM
Ignite Modification Date:
2025-12-25 @ 3:20 AM
NCT ID:
NCT03109405
Eligibility Criteria:
Inclusion Criteria:
* Subject ≥ 18 years of age
* Subject with history of failed venous access, venipuncture, or IV cannula placement
* Subject agreed to required follow-up
* Subject provided written, informed consent
Exclusion Criteria:
* Subject currently had compromised skin on either forearm or hand
* Subject currently on any blood thinning medication other than 81mg of aspirin
* Subject had been diagnosed with peripheral neuropathy, has had a complex fracture or surgery in the forearm, or has other condition that diminishes sensation in one or both arms, hands or fingers
* Subject had a demand type pacemaker or defibrillator
* Subject is female of child-bearing potential and had a positive urine pregnancy test
* Subject had a history of seizure, convulsions or epilepsy
* Subject had a known allergy to Epsom salts
* Subject had any other condition that may affect the ability to complete study requirements
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03109405
Study Brief:
Protocol Section:
NCT03109405