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Screening |
Treatment One |
Treatment Two |
Treatment Three |
Follow Up |
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Screening 1 |
Screening 2 |
Baseline |
Week 2 |
Week 4 |
Week 6 |
Week 8 |
Week 8 |
Week 12 |
Week 12 |
Week 16 |
Week 16 |
Week 20 |
Week 20 |
Week 24 |
Week 26 |
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Screen One |
Screen Two |
Dose |
Week 2 |
Week 4 |
Week 6 |
Week 8 |
Week NPI |
Week 12 |
Week 12 NPI |
Week 16 |
Week 16 NPI |
Week 20 |
Week 20 NPI |
Week 24 |
Week 26 |
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-4..0 hours |
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-3..3 days |
-3..3 days |
-3..3 days |
-3..3 days |
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-4..4 days |
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-4..4 days |
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-4..4 days |
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-4..4 days |
-3..3 days |
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Informed consent |
X |
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Inclusion and exclusion criteria |
X |
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Patient number assigned |
X |
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Demographics |
X |
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Hachinski Ischemic Scale |
X |
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MMSE |
X |
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Physical examination |
X |
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X |
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Medical history |
X |
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Habits |
X |
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Chest X-ray |
X |
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Apo E genotyping |
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X |
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Patient randomised |
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X |
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Vital Signs and Temperature |
X |
X |
X |
X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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Ambulatory ECG placed |
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X |
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Ambulatory ECG removed |
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X |
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ECG |
X |
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X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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Placebo TTS test |
X |
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CT scan |
X |
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Concomitant medications |
X |
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X |
X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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Hematology |
X |
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X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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Chemistry |
X |
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X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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Uninalysis |
X |
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X |
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X |
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X |
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Plasma Specimen (Xanomeline) |
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X |
X |
X |
X |
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X |
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X |
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Hemoglobin A1C |
X 1 |
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Study drug record , Medications dispensed, Medications returned |
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X |
X |
X |
X |
X |
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X |
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X |
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X |
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X |
X |
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TTS Acceptability Survey |
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X |
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ADAS-Cog |
X 2 |
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X |
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X |
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X |
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X |
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CIBIC+ |
X 2 |
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X |
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X |
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X |
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X |
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DAD |
X 2 |
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X |
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X |
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X |
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X |
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NPI-X |
X 2 |
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X |
X |
X |
X |
X |
X |
X |
X |
X |
X |
X |
X |
X |
X |
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Adverse events |
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Check adverse events |
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Subject supine |
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Vital signs while supine |
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Subject Standing |
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Vital signs while standing |
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| 1 | Performed if patient is an insulin-dependent diabetic |
| 2 | Practice only - It is recommended that a sampling of the CIBIC+, ADAS-Cog, DAD, and NPI-X be administered at Visit 1. Data from this sampling would not be considered as study data and would not be collected. |