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Study on brain structural MRI in post traumatic stress disorder patients who lost child

Study on brain structural MRI in post traumatic stress disorder patients who lost child.

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018430
Enrollment
Unknown
Registered
2018-09-18
Start date
2018-10-07
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

Post-traumatic stress disorder

Interventions

Case group:Functional magnetic resonance examination
Control group:Functional magnetic resonance examination

Sponsors

First Affiliated Hospital of Medical College, Shihezi University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 58 Years

Inclusion criteria

Inclusion criteria: 1. PTSD diagnostic criteria in the Diagnostic and Statistical Manual of Mental Disorders (Fourth Edition, Text Rev-ision, DSM-IV), post-traumatic stress disorder screening questionnaire (Posttraumatic Stress Disorder Check-list-Civilian Version, PCL-C) = 41 points; 2. aged 18-58 years old male and female; 3. primary school education level, Webster Adult Intelligence Scale (WAIS-R) = 80 points; 4. patients who did not receive psychoseptic therapy for at least two weeks before enrollment; 5. no history of alcohol and drug abuse; 6. no abnormalities in EEG and physical examination results; 7. right hand; 8. clear consciousness and willing to accept All kinds of questionnaires and scales surveyors; 9. operation examinations have obtained the informed consent of the subjects or their guardians, in line with ethical standards.

Exclusion criteria

Exclusion criteria: 1. previous history of traumatic brain injury, nervous system diseases and serious physical diseases; 2. history of mental disorders caused by substance abuse, severe psychosis and mental retardation; 3. metal implants in vivo; 4. within 2 months before enrollment Treated with psychoactive drugs; 5. pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Gray matter volume;

Countries

China

Contacts

Public ContactZhang Guiqing

First Affiliated Hospital of Medical College, Shihezi University, Shihezi, Xinjiang

firstli@126.com+86 13999732539

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026