Skip to content

D-cycloserine Adjunctive Treatment for Posttraumatic Stress Disorder (PTSD) in Adolescents

D-cycloserine Adjunctive Treatment for PTSD in Adolescents

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01157429
Enrollment
24
Registered
2010-07-07
Start date
2010-06-30
Completion date
2012-06-30
Last updated
2017-06-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Posttraumatic Stress Disorder, PTSD

Keywords

Cognitive Behavior Therapy, Children, Adolescents, Pharmacotherapy

Brief 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.

Interventions

DRUGD-cycloserine

D-cycloserine 50 mg by mouth prior to sessions 5-12 of the 12-session CBT protocol.

DRUGPlacebo pill

Placebo pill by mouth prior to sessions 5-12 of teh 12-session CBT protocol.

BEHAVIORALCBT

12-session CBT protocol, called Youth PTSD Treatment.

Sponsors

National Alliance for Research on Schizophrenia and Depression
CollaboratorOTHER
Tulane University School of Medicine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Certain number of PTSD symptoms plus functional impairment * Must be able to swallow pills

Exclusion criteria

* Serious kidney or liver disease * Epilepsy * Bipolar disorder * Psychosis

Design outcomes

Primary

MeasureTime frameDescription
Child PTSD Symptom Scale (CPSS)After 12 therapy sessions, up to 28 weeks.The CPSS is a 17-item standardized, self-administered questionnaires with versions for both youths and caregivers. Items are scored on 0-3 scale. Minimum possible score is 0 and maximum is 51. Only the total score is used; there are no subscales. A higher score indicates greater symptom severity (worse).

Countries

United States

Participant flow

Pre-assignment details

A total of 63 youth were assessed. Only 47 meet all the inclusion and exclusion criteria and were offered treatment. Of those 47, only 24 were retained through session 5 of the treatment, which was the point of random allocation. Twenty-three subjects of the 47 subjects who were offered treatment dropped out prior to session 5.

Participants by arm

ArmCount
D-cycloserine Plus CBT
Individuals receive 12 sessions of manualized trauma-focused cognitive behavioral therapy plus seven doses of D-cycloserine. D-cycloserine: D-cycloserine 50 mg by mouth prior to sessions 5-12 of the 12-session CBT protocol.
12
Placebo Pill
Individuals receive 12 sessions of trauma-focused cognitive behavioral therapy plus seven doses of placebo pill. Placebo pill: Placebo pill by mouth prior to sessions 5-12 of the 12-session CBT protocol.
12
Total24

Baseline characteristics

CharacteristicD-cycloserine Plus CBTPlacebo PillTotal
Age, Continuous15.7 years
STANDARD_DEVIATION 1.6
15.9 years
STANDARD_DEVIATION 1.7
15.8 years
STANDARD_DEVIATION 1.6
Region of Enrollment
United States
12 participants12 participants24 participants
Sex: Female, Male
Female
10 Participants7 Participants17 Participants
Sex: Female, Male
Male
2 Participants5 Participants7 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
1 / 122 / 12
serious
Total, serious adverse events
0 / 120 / 12

Outcome results

Primary

Child PTSD Symptom Scale (CPSS)

The CPSS is a 17-item standardized, self-administered questionnaires with versions for both youths and caregivers. Items are scored on 0-3 scale. Minimum possible score is 0 and maximum is 51. Only the total score is used; there are no subscales. A higher score indicates greater symptom severity (worse).

Time frame: After 12 therapy sessions, up to 28 weeks.

ArmMeasureValue (MEAN)Dispersion
D-cycloserine Plus CBTChild PTSD Symptom Scale (CPSS)20.4 units on a scaleStandard Deviation 9.7
Placebo PillChild PTSD Symptom Scale (CPSS)11.0 units on a scaleStandard Deviation 8.9

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026