Clinical TrialID 6722

Prolonged Exposure for Post Traumatic Stress Disorder (PTSD) With/Without Yohimbine

NCT01031979

Post-Traumatic Stress Disorder

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Record Fields

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Clinical Trial Id
6722
Evidence Id
6722
Core Evidence Id
6722
Source Clinical Trial Id
6709
Herb2 Clinical Trial Id
HBCT006709
Nct Id
NCT01031979
Title
Prolonged Exposure for Post Traumatic Stress Disorder (PTSD) With/Without Yohimbine
Status
Completed
Phase
Phase 2
Study Result
Yes
Study Condition
Post-Traumatic Stress Disorder
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
Intervention
DRUG: Yohimbine|DRUG: Placebo
Intervention Allocation
Randomized
Intervention Model
Parallel
Intervention Mask
Quadruple
Intervention Purpose
Treatment
Gender
Male
Age
Adult
Enrollment
26
Outcome Measure
Trauma-Cued Heart Rate Reactivity, The primary outcome was trauma-cued heart rate reactivity a week after the drug visit as measured by the PTSD Brief Reactivity (PBR) task. For each patient, a 3-minute trauma script was constructed containing vivid details of the target trauma and used in tandem with a standard neutral script for baseline measurement. Heart rate reactivity for each time point was the beats per minute (BPM) difference between the neutral and trauma scripts represented as a slope., One week after drug visit
Sponsor Collaborator
VA Office of Research and Development
Funded By
FED
Location
Ralph H. Johnson VA Medical Center, Charleston, SC, Charleston, South Carolina, 29401-5799, United States
Other Id
CDA-2-013-09F
Start Date
2010-12-01
Primary Completion Date
2015-04-01
Completion Date
2015-07-07
First Posted
2009-12-15
Results First Posted
2017-02-24
Last Update Posted
2018-02-07
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01031979
Title Cn
Title En
Prolonged Exposure for Post Traumatic Stress Disorder (PTSD) With/Without Yohimbine
Bilingual Status
semi_complete