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 @ 12:06 AM
Ignite Modification Date:
2025-12-25 @ 12:06 AM
NCT ID:
NCT00357058
Eligibility Criteria:
* INCLUSION CRITERIA:
Normal volunteers who are willing and able to remain relaxed and immobile during active scans, for a period of up to 2 hours.
EXCLUSION CRITERIA:
Subjects with: metal in the cranium except for crowns or fillings in mouth and permanent metal dental braces, metal fragments from occupational exposure or surgical clips in or near the brain.
Subjects with eye, blood vessel, cochlear or eye implants, with increased intracranial pressure as evaluated by clinical means, with cardiac or neural pacemakers, intracardiac lines and/or implanted medication pumps.
Subjects with large hemorrhagic or brain stem stroke.
Subjects with multiple cerebral lesions with residual deficits.
Subjects with history of head injury with loss of consciousness.
Subjects with history of severe alcohol or drug abuse or psychiatric illness.
Subjects with unstable cardiac dysrhythmia or unresponsive arterial hypertension (greater than 160/100 mmHg).
Subjects with history of hyperthyroidism or individuals receiving drugs acting primarily on the central nervous system or disorders of the blood coagulation system.
Subjects with excessive callus at their fingers.
Preganant women will be excluded from the study.
SUBJECTS DISCONTINUATION CRITERIA:
Subject's poor compliance with protocol evaluations or examinations and subject's request to withdraw.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00357058
Study Brief:
Protocol Section:
NCT00357058