Trials / Completed
CompletedNCT01157429
D-cycloserine Adjunctive Treatment for Posttraumatic Stress Disorder (PTSD) in Adolescents
D-cycloserine Adjunctive Treatment for PTSD in Adolescents
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 24 (actual)
- Sponsor
- Tulane University School of Medicine · Academic / Other
- Sex
- All
- Age
- 13 Years – 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to show whether D-cycloserine in combination with cognitive behavioral therapy (CBT) is more effective than CBT plus placebo to reduce symptoms of posttraumatic stress disorder (PTSD) in 13-18 year-old children.
Detailed description
While most individuals with PTSD treated with cognitive behavioral therapy (CBT) show improvement, they still have some enduring symptoms and functional impairment. Accordingly, there is a need for treatment advances. D-cycloserine (DCS), an antibiotic that has been used for over 50 years, has also been found to have positive effects on cognition and anxiety. DCS was found to enhance learning and memory, and also facilitates extinction of fear reactions. However, DCS only produces an extinction effect when paired with behavioral training, not when simply given alone. Thus, the medication only needs to be given for seven doses in this research and youth do not need to take the medication long term. The research also includes a three-month follow-up.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | D-cycloserine | D-cycloserine 50 mg by mouth prior to sessions 5-12 of the 12-session CBT protocol. |
| DRUG | Placebo pill | Placebo pill by mouth prior to sessions 5-12 of teh 12-session CBT protocol. |
| BEHAVIORAL | CBT | 12-session CBT protocol, called Youth PTSD Treatment. |
Timeline
- Start date
- 2010-06-01
- Primary completion
- 2012-06-01
- Completion
- 2012-06-01
- First posted
- 2010-07-07
- Last updated
- 2017-06-06
- Results posted
- 2017-06-06
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01157429. Inclusion in this directory is not an endorsement.