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A randomised double-blind placebo-controlled pilot study of D-cycloserine-augmented exposure therapy in adolescents with obsessive-compulsive disorder

A randomised double-blind placebo-controlled pilot study of D-cycloserine-augmented exposure therapy in adolescents with obsessive-compulsive disorder

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2008-006947-38-GB
Enrollment
24
Registered
2009-07-09
Start date
2009-01-15
Completion date
Unknown
Last updated
2018-12-04

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

Conditions

Obsessive-compulsive disorder (OCD) MedDRA version: 9.1 Level: LLT Classification code 10029898 Term: Obsessive-compulsive disorder

Interventions

Trade Name: Cycloserine Pharmaceutical Form: Capsule* Other descriptive name: D-cycloserine Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 50- Pharmaceutical form

Sponsors

King's College London (Institute of Pyschiatry)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: i) DSM-IV diagnosis of OCD ii) Age 12-18 iii) Referred to the National and Specialist OCD clinic at Maudsley Hospital iv) If on medication, that should be stable for 12 weeks, and not be changed during the course of the trial v) Provision of written informed consent (patient and carer) Are the trial subjects under 18? yes Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) no F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: i) Current diagnosis of psychosis, current alcohol or substance abuse/dependence ii) English too poor to engage in treatment iii) Severe disabling neurological disorder iv) Medical contraindication to cycloserine, including epilepsy and porphyria v) A diagnosed global learning disability or pervasive developmental disorder vi) Characteristics interfering with completion of treatment eg life-threatening or unstable medical illness vii) Pregnancy viii) Not suitable for CBT (selective mutism, lack of insight or motivation to change)

Design outcomes

Primary

MeasureTime frame
Main Objective: To establish the clinical effectiveness of D-cycloserine (DCS) augmented cognitive behavioural therapy (CBT) for children and adolescents with OCD, and whether that affects the speed of recovery. ;Secondary Objective: To determine which processes in fear extinction are modified by DCS, and when this occurs, during exposure therapy for OCD in young people. ;Primary end point(s): Childrens' Yale-Brown Obsessive-Compulsive Scale (CY-BOCS)

Countries

United Kingdom

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026