NCT01680107
Terminated
Phase 3
The Effect of a Single-dose of D-cycloserine on the Basic Effects of Cognitive-behaviour Therapy for Panic Disorder - a Randomized Placebo-controlled Trial
ConditionsPanic Disorder
Overview
- Phase
- Phase 3
- Intervention
- d-cycloserine
- Conditions
- Panic Disorder
- Sponsor
- University of Oxford
- Enrollment
- 33
- Locations
- 1
- Primary Endpoint
- self-reported and clinician-rated anxiety and depression measures
- Status
- Terminated
- Last Updated
- 8 years ago
Overview
Brief Summary
The purpose of this study is to determine whether d-cycloserine augments the clinical effects of exposure-based cognitive-behaviour therapy for panic disorder.
Investigators
Eligibility Criteria
Inclusion Criteria
- •clinical diagnosis of panic disorder
- •at least moderate agoraphobic avoidance
Exclusion Criteria
- •psychoactive medication last 6 weeks
- •exposure-based cognitive-behaviour treatment for panic disorder and agoraphobia during last 3 months
- •female participant who is pregnant or breast-feeding
- •lifetime history of psychosis, bipolar disorder, alcohol, medication or drug abuse or dependence; current primary depressive disorder
- •lifetime history of epilepsy or other significant disease or disorder
Arms & Interventions
d-cycloserine
oral, capsule, 250 mg, once
Intervention: d-cycloserine
d-cycloserine
oral, capsule, 250 mg, once
Intervention: cognitive-behaviour therapy
sugar pill
oral, capsule, once
Intervention: placebo
sugar pill
oral, capsule, once
Intervention: cognitive-behaviour therapy
Outcomes
Primary Outcomes
self-reported and clinician-rated anxiety and depression measures
Time Frame: 6 months
Secondary Outcomes
- emotional information processing(1 day)
Study Sites (1)
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