Propranolol in Post Traumatic Stress Disorder
Information source: University Hospital, Toulouse
Information obtained from ClinicalTrials.gov on November 03, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Post-Traumatic Stress Disorder
Intervention: propranolol (Drug)
Phase: Phase 2
Sponsored by: University Hospital, Toulouse
Official(s) and/or principal investigator(s):
Philippe BIRMES, Principal Investigator, Affiliation: University Hospital, Toulouse
Problem and Objectives: There is currently no pharmacological treatment for curing post
traumatic stress disorder (PTSD). The investigators will test whether propranolol when given
immediately after trauma evocation is able to decrease the strength of the traumatic memory,
and by extension, the severity of PTSD symptoms associated with that memory.
1. The subjects will show a significant pre/post decrease in PTSD symptoms.
2. Those gains will be maintained at follow-up.
Study Design: Open pharmacological trial.
Method: On the first visit (V1), the subjects will describe their traumatic experience in
writing and will receive the propranolol. A script describing this experience will be
constructed to be used in the subsequent encounters to elicit the trauma memory. A week later
(V2), before receiving the propranolol, subjects will be asked to read aloud their trauma
script while imagining it as vividly as possible for 10 minutes. This weekly treatment will
be repeated 6 times (from V1 to V6). A total of 6 doses of propranolol will be given. A
self-report measure will be used to monitor improvement in PTSD symptomatology on the
following visits: V1, V4, V6, V7 and V8 (3 month follow-up).
Statistical Analyses: A repeated measure ANOVA (pre-test, post-test, and 3-month follow-up)
using the PTSD symptom score will be conducted.. Three t-tests will be performed to examine
simple effects. The alpha level will be set at p = .05 (two-tailed). Fisher's exact test will
be used to examine whether Ss still meet the diagnostic criteria for PTSD at the end of the
Clinical Implications: If this treatment is effective, a randomized controlled trial will be
launched. This treatment has the potential to become the first pharmacological treatment
designed to cure PTSD.
Official title: Reduction of the Traumatic Memory by Reconsolidation Blockade: A Pilot Study
Study design: Treatment, Open Label, Uncontrolled, Single Group Assignment, Efficacy Study
Primary outcome: PTSD Checklist score
Secondary outcome: SCID diagnosis
Minimum age: 18 Years.
Maximum age: 65 Years.
- 18-65 years old
- Suffer from AZF-related PTSD (PCL score more than 44)
- Sign consent form
- Subjects must have health coverage.
- Not diagnosed with current, chronic AZF-related PTSD
- Age < 18 or > 65
- Systolic blood pressure < 100 mm Hg
- Medical condition that contraindicates the administration of propranolol, e. g.,
history of congestive heart failure, heart block, insulin-requiring diabetes, chronic
bronchitis, emphysema, or asthma. With regard to asthma, because many persons who say
they have had an asthma attack, especially as a child, may only have had hay fever,
another allergy, or another non-asthmatic episode, a blanket exclusion criterion may
be overly restrictive. Therefore, asthma attacks will only be exclusionary if they:
- occurred within the past ten years,
- occurred at any time in life if induced by a β-blocker, or
- are currently being treated, regardless of the date of last occurrence.
Cardiological consultation will be obtained as necessary.
- Previous adverse reaction to, or non-compliance with, a β-blocker
- Current use of medication that may involve potentially dangerous interactions with
propranolol, including, other β-blockers, antiarrhythmics, calcium channel blockers,
and potent P450 2D6 inhibitors, e. g., fluoxetine, paroxetine, miconazole, sulconazole,
metoclopramide, quinidine, ticlopidine, and ritonavir.
- Contraindicating psychiatric condition, including lifetime or current psychotic,
bipolar, melancholic, or substance dependence or abuse disorder; suicidality.
- Initiation of, or change in, psychotropic medication within the previous two months.
For subjects receiving stable doses of pharmacotherapy, they and their providers will
be asked not to change the regimen except in clinically urgent circumstances; if this
becomes necessary, a decision will be made on a case-by-case basis with regard to
retaining the subject or terminating participation.
- Current participation in any psychotherapy (other than strictly supportive). Subjects
will be asked not to initiate psychotherapy during the course of the proposed study
except in clinically urgent circumstances; if this becomes necessary, a decision will
be made on a case-by-case basis with regard to retaining the subject or terminating
- Inability to understand the study's procedures, risks, and side effects, or to
otherwise give informed consent for participation
- Does not understand French
Locations and Contacts
Psychiatric Department, Toulouse 31059, France; Recruiting
Philippe BIRMES, MD, Phone: 33-561772581
Philippe BIRMES, MD, Principal Investigator
Rémy Klein, MD, Sub-Investigator
Alain Brunet, PhD, Sub-Investigator
Laurent SCHMITT, PhD, Sub-Investigator
Pitman RK, Sanders KM, Zusman RM, Healy AR, Cheema F, Lasko NB, Cahill L, Orr SP. Pilot study of secondary prevention of posttraumatic stress disorder with propranolol. Biol Psychiatry. 2002 Jan 15;51(2):189-92.
Vaiva G, Ducrocq F, Jezequel K, Averland B, Lestavel P, Brunet A, Marmar CR. Immediate treatment with propranolol decreases posttraumatic stress disorder two months after trauma. Biol Psychiatry. 2003 Nov 1;54(9):947-9. Erratum in: Biol Psychiatry. 2003 Dec 15;54(12):1471.
Starting date: April 2007
Ending date: November 2008
Last updated: July 30, 2008