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Tachikawa Project for Prevention of Posttraumatic Stress Disorder With Polyunsaturated Fatty Acid (TPOP): TPOP-01 Study

Phase 2 Study of Tachikawa Project for Prevention of Posttraumatic Stress Disorder With Polyunsaturated Fatty Acid (TPOP): TPOP-01 Study

Status
Completed
Phases
Phase 1Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00671489
Enrollment
15
Registered
2008-05-05
Start date
2008-05-31
Completion date
2009-02-28
Last updated
2012-07-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Trauma, Posttraumatic Stress Disorder

Keywords

Patients, high-energy, admitted, intensive care unit, motor vehicle accident, falling from height, other accident

Brief summary

The purpose of this study is to evaluate the efficacy and safety of Polyunsaturated Fatty Acid for the prevention of Posttraumatic Stress Disorder (PTSD) in patients with accidental injuries.

Detailed description

Accidental injuries, mostly motor vehicle accident, in civilian population are frequent events. For instance, nearly one-third of injured patients appear to develop trauma-related psychiatric illness and the major diagnoses are post-traumatic stress disorder (PTSD) and depressive disorder. Omega-3 Polyunsaturated Fatty Acid (Omega-3 PUFA) has some evidence of efficacy of treatment in patients with anxiety and mood disorders, but no evidence of preventing anxiety and mood disorders that occur subsequent to accidental injuries. We evaluate efficacy and safety of Omega-3 PUFA for the secondary prevention of Posttraumatic Stress Disorder (PTSD) and related psychiatric illness in patients with accidental injury.

Interventions

A capsule of omega-3 Polyunsaturated Fatty Acid, 300mg (including 70% docosahexaenoic acid, 7% eicosapentaenoic acid and other), 7 capsules per day in 12 week.

Sponsors

University of Toyama
CollaboratorOTHER
Chiba University
CollaboratorOTHER
Japan Science and Technology Agency
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. 18 plus years 2. A native Japanese speaking ability 3. Possibility 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 ≦ γGTP 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

Design outcomes

Primary

MeasureTime frame
Total score of Clinician-Administrated PTSD Scale (CAPS)Three month

Secondary

MeasureTime frame
DL-serineThree month, one month
ActivinThree month, one month
Number of days of leave taken from the time of injuryThree month
Buss-Perry Aggression Questionnaire (BAQ)Three month, one month, baseline
Total score of Clinician-Administrated PTSD Scale (CAPS)One month
DHEA: dehydroepiandrosteroneThree month, one month
NPY: neuropeptide YThree month, one month
IL-1 beta: interleukin 1 betaThree month, one month
IL-6: interleukin 6Three month, one month
TNF alpha: tumor necrosis factor alphaThree month, one month
L-serineThree month, one month
Incidence of diagnosis of PTSD (including partial PTSD)Three month, one month
Total score of Montgomery Asberg Depression Rating Scale (MADRAS)Three month, one month
Incidence of depression evaluated by Mini-International Neuropsychiatric Interview (MINI)Three month, one month
Autonomic response measured before, during and after script driven imagery and acoustic stimulationThree month
Score of Impact of Event Scale revised (IES-R)Three month, one month
Score of Hospital Anxiety and Depression scale (HADS)Three month, one month
Score of health related Quality of Life scale, SF-36Three month, one month
Score of Conner-Davidson Resilience Scale (CD-RISC)Three month, one month
Brain-derived neurotrophic factor (BDNF) in serumThree month, one month
D-serineThree month, one month

Countries

Japan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026