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Completed

NCT Number: NCT01569685

The Treatment of Traumatised Refugees With Sertraline Versus Venlafaxine in Combination With Psychotherapy

Background: The treatment of traumatised refugees is one of the areas within the field of psychiatry with the weakest evidence for the different types of treatment. This is a problem for both patients and doctors as well as for society.

The treatment of choice today for Post Traumatic Stress disorder (PTSD) is antidepressants from the subgroup of Selektive Serotonin Reuptake Inhibitors (SSRI), among these the drug Sertraline. The evidence for the use of these drugs as treatment for chronically complex PTSD in traumatised refugees is however very limited and a large part of the group is estimated to be insufficiently treated with this type of medicine. Venlafaxine is an antidepressant from the subgroup of dual action product which means that is works on several pathways in the brain. Among others it influences the area in the brain that is responsible for the enhanced anxiety and hyperarousal experienced by traumatised refugees and which is found to be enlarged among patients suffering from PTSD.

All together there is not sufficient evidence to conclude which type of medical and psychological treatment that is most efficient when it comes to the treatment of traumatised refugees. Also there is a lack of studies which examines social functioning and the relation between psychosocial resources and outcome from treatment. Furthermore there is a lack of knowledge of predictors of treatment outcome for the individual patients. This study seeks to produce some of this evidence.

Method: This study is expected to include approximately 150 patients randomised into two different groups. The patients are treated with Setraline or Venlafaxine depending on the group the randomised to. Patients in both groups are getting the same version of manual based Cognitive Behavioural Therapy that is specially adapted to this group of patients. The treatment period is 6-7 month. The trial endpoints are PTSD-and depression symptoms and social functioning all measured on internationally validated ratings scales.

Furthermore the study will examine the relation between expected outcome of treatment from a range of predictors and the actual treatment results for the individual patient.

Results: Altogether this study will bring forward new standards for clinical evaluation and treatment of traumatised refugees and the results are expected to be used in reference programmes/clinical guidelines.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Competence Center for Transcultural Psychiatry

Gentofte Municipality, 2900, Denmark

About this study

Please see the summary above

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients referred to treatment in Psychiatric Clinic for refugees, Psychiatric Center Ballerup between April 2012 to May 2013
  • Adults (18 years or older)
  • Refugees or reunified with a refugee spouse
  • Symptoms of PTSD defined by ICD-10 research criterias.
  • Previosly traumatized
  • Motivated for treatment
  • Informed consent

Exclusion criteria

  • Psychotic disorder (ICD-10 diagnosis F2x og F30.1-F309)
  • Active substance abuse (ICD-10 F1x.24-F1x.26).
  • In need of acute admission to psychiatric hospital)
  • No informed consent
  • Pregnant women, breastfeeding women or women who wish to become pregnant within the project period.

Treatment and study plan

Venlafaxine

Drug

Tablets, once a day, max 375 mg day (maximal recommended dose)

Other names: Efexor

Sertraline

Drug

Tablets, once a day, maximum 200 mg/day (maximum required dose)

Primary outcomes

  1. Harvard Trauma Questionnaire (HTQ)

    Time frame: Change from baseline after aprox. 6 months treatment

    Self administered Rating Scale

Secondary outcomes

  1. Hopkins Symptom Check List (HSCL-25)

    Time frame: Change from baseline after aprox. 6 months treatment

  2. Social Adjustment Scale Self Report (SAS-SR) short version

    Time frame: Change from baseline after aprox. 6 months treatment

  3. Hamilton Depresssion Scale (17 items)

    Time frame: Change from baseline after aprox. 6 months treatment

  4. Hamilton Anxiety Scale (14 items)

    Time frame: Change from baseline after aprox. 6 months treatment

Sponsors and collaborators

Lead sponsor

Charlotte Sonne

Other

Collaborators

  • Psychiatric Center Ballerup

Registry information

Official study title

The Treatment of Traumatised Refugees With Sertraline Versus Venlafaxine in Combination With Psychotherapy - a Randomised Clinical Study

Acronym: PTF3

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Apr 3, 2012
Registry last updated
Mar 4, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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