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Treatment of exacerbations of post-traumatic stress disorder by short-term dexamethasone, a pilot study.

Conditions
Posttraumatic stress syndrome F431
Registration Number
EUCTR2010-018486-37-SE
Lead Sponsor
Kris-och Traumacentrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Authorised-recruitment may be ongoing or finished
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Excacerbation in chronic ptsd with marked flash-backs.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

1.Suicidal risk
2.Bipolar disease
3.Psycosis with lack of reality testning
4.Aggression
5.Sociopati
6.Infection
7.Untreated ulcus

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: Investigate if dexamethasone-treatment reduces symtoms in patients with excacerbation of chronic ptsd.;Secondary Objective: Investigate if dexamethasone-treatment reduces symtoms related to depression and dissociation. <br><br>;Primary end point(s): Changes in self evaluation scores of PTSD-symtoms (Davidson Trauma Scale).
Secondary Outcome Measures
NameTimeMethod
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