F43.1
Conditions
Interventions
Group 1: 24 IE Oxycotin intranasal
Group 2: Placebo intranasal
Sponsors
Klinikum rechts der Isar der TU München
Eligibility
Sex/Gender
Female
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Prevalence of posttraumatic stress disorder
Exclusion criteria
Exclusion criteria: Pregnancy, medication with beta-blockers, known cardiovascual diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Heart rate increase relative to baseline during listening to an individualized trauma script (assessed by impedance cardiography). | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective distress during listening to an individualized trauma script (Global scale 0-10) and Response to Script Driven Imagery Scale | — |
Countries
Germany
Contacts
Public ContactMartin Sack
Klinik für Psychosomatische Medizin und Psychotherapie, Klinikum rechts der Isar, Technische Universität München
Outcome results
None listed