NCT01020695

Brief Summary

In this study the Quantitative Electroencephalography and low resolution topographic analysis of chronic Post-traumatic stress disorder and normal subjects will be compared.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
10

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Nov 2009

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2009

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2009

Completed
22 days until next milestone

First Submitted

Initial submission to the registry

November 23, 2009

Completed
2 days until next milestone

First Posted

Study publicly available on registry

November 25, 2009

Completed
Last Updated

November 7, 2012

Status Verified

November 1, 2012

Enrollment Period

Same day

First QC Date

November 23, 2009

Last Update Submit

November 6, 2012

Conditions

Post-Traumatic Stress Disorder

Keywords

PTSDEEGQEEGLORETA

Study Arms (2)

PTSD veterans

18 PTSD veterans

controls

20 controls

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Veterans with chronic PTSD of at least 2 years.

You may qualify if:

  • veterans suffering for PTSD according to the DSM-IV-TR for at least 2 years.
  • The 10 age matching controls will be recruited from the Beer Sheva mental stuff.

You may not qualify if:

  • Without any neurological or head trauma.
  • Without alcohol or substance abuse.
  • No evidence of psychotic episode in there history.
  • Stable doses of different specific serotonin reuptake inhibitors (SSRI) antidepressant for at least two months.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Beer Sheva Mental Health Center

Beersheba, Israel

Location

MeSH Terms

Conditions

Stress Disorders, Post-Traumatic

Condition Hierarchy (Ancestors)

Stress Disorders, TraumaticTrauma and Stressor Related DisordersMental Disorders

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr.

Study Record Dates

First Submitted

November 23, 2009

First Posted

November 25, 2009

Study Start

November 1, 2009

Primary Completion

November 1, 2009

Study Completion

November 1, 2009

Last Updated

November 7, 2012

Record last verified: 2012-11

Locations

IL(1)