Clinical Trial Details
Braintumor Website

[Information provided by: ClinicalTrials.gov, which provides patients, family members, and members of the public easy and free access to information on clinical studies for a wide range of diseases and conditions.]

NCT00671099 : Tachikawa Project for Prevention of Posttraumatic Stress Disorder With Polyunsaturated Fatty Acid (TPOP): TPOP-02 Study
PhasePhase 3
AgesMin: 18 Years Max: N/A
Eligibility
Inclusion Criteria:

1. 18 plus years

2. A native Japanese speaking ability

3. Possibility to contact patients with injury in 240 hours, and dosing in oral use

4. Physical and metal status to possible understands scope and contents in the trial and
gets informed consent

Exclusion Criteria:

1. Clearly irretrievable acute brain parenchyma damage and subdural or subarachnoidal
bleeding detected by computed tomography and/or magnetic resonance imaging

2. Cognitive impairment: Mini Mental State Examination < 24

3. Heavy drinker or 100IU/L ? ?GTP in administration

4. Heavy smoker (over 40 cigarettes per day)

5. History and current suspicion in diagnosis of psychosis and bipolar I disorder

6. Suspicion in diagnosis of alcoholic, substance-related disorder and eating disorder

7. Existence of marked serious symptoms such as suicidal ideation, self-harm behavior,
dissociation, status of need rapidly psychiatric treatment

8. Use of anti-epilepsy drug, lithium, ethyl icosapentate and anti-coagulant drug (for
example, aspirin, warfarin, etc) within 3 month at regular intervals

9. Use of polyunsaturated fatty acid supplement within 3 month at regular intervals

10. Habit of eating fish over 4 times per week
LinksPermanent Link to THIS page: https://virtualtrials.com/nct/display1trial.cfm?nct=NCT00671099      |      Link to official Clinicaltrials.gov listing
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