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 @ 2:46 AM
Ignite Modification Date:
2025-12-25 @ 2:46 AM
NCT ID:
NCT01386333
Eligibility Criteria:
Inclusion Criteria:
* Age 30-80 years
* Meets "Neary criteria" for diagnosis of probable frontotemporal dementia
* Neuroimaging (CT, MRI or SPECT scan) supports diagnosis of frontotemporal dementia
* Provides written informed consent and has a caregiver or legally acceptable representative who provides written informed consent.
Exclusion Criteria:
* Has a history of a myocardial infarction within the last two years or congestive heart failure.
* Current uncontrolled hypertension
* Current bradycardia (rate \< 50 beats per minute/bpm) or tachycardia (rate \> 100 bpm)
* Current hyponatremia
* Current use of prostaglandin medications
* Females who are pregnant or breastfeeding
* Use of any investigational or experimental drug or device within the last 60 days prior to screening or within 5 half-lives of the experimental drug , whichever is longer.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
30 Years
Maximum Age:
80 Years
Study:
NCT01386333
Study Brief:
Protocol Section:
NCT01386333