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 @ 2:16 AM
Ignite Modification Date:
2025-12-25 @ 2:16 AM
NCT ID:
NCT01646060
Eligibility Criteria:
Inclusion Criteria:
* Written informed consent
* Male, 18-65 years of age
* Subject is suitable for a blood draw of a pint of blood
* Weighs at least 110 pounds
Exclusion Criteria:
* Subject has a heart condition that may interfere with the Zynex CM-1500
* Subject has unstable or untreated heart disease
* Subject has been diagnosed with chronic fatigue syndrome
* Subject is taking coumadin (warfarin), heparin, or other prescription blood thinners for at least 7 days prior to blood draw
* Subject donated blood within 8 weeks prior to blood draw
* Subject has high or low blood pressure on the day of blood draw
* Subject hemoglobin \< 12.5 g/dL
Healthy Volunteers:
True
Sex:
MALE
Minimum Age:
18 Years
Maximum Age:
65 Years
Study:
NCT01646060
Study Brief:
Protocol Section:
NCT01646060