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Phase 2 N=54 Randomized Triple-blind Treatment

fMRI Study Examining Effects of D-cycloserine in Specific Phobia

Phobias

Enrolled (actual)
54
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcome: Primary: fMRI Brain Activations During Symptom Provocation — .200; .157; -.013; .036 percent signal change

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
D-cycloserine (Drug); Placebo (Drug)
Age
Adult · 18+ yrs
Sex
All
Sponsor
University of Kansas Medical Center
Primary completion
Dec 2012

Outcome Measures

OutcomeResultp-value
PRIMARY
fMRI Brain Activations During Symptom Provocation
.200; .157; -.013; .036; .012; .021
SECONDARY
Cognitive Functioning Measured Using the Wechsler Memory Scale III (Logical Memory and Faces Subtests)
51.93; 49; 52.69; 52.93; 34.36; 32.46
SECONDARY
Cognitive Functioning Measured Using the Rey-Osterrieth Complex Figure Test (RCFT)
4.93; 4.92; 3.69; 4.14; 34.68; 34.46
SECONDARY
Cognitive Functioning Measured Using the Iowa Gambling Test
44.29; 32.62; 28.58; 21.85
SECONDARY
Cognitive Functioning Measured Using the Wisconsin Card Sorting Task
13.29; 13.62; 18.23; 15.67

Summary

The research team hopes to use brain imaging and mental testing to learn more about specific phobias and the treatment of phobia. When given directly prior to therapy sessions, D-cycloserine has been shown to enhance the effects of therapy. This study hopes to identify reasons why D-cycloserine has this effect by measuring brain activity.

Eligibility Criteria

Inclusion Criteria

  • Right-handed
  • Adults between 18 and 55 years of age
  • Subjects in the phobic group will additionally meet diagnostic (DSM-IV) criteria for spider phobia.
  • Individuals of both genders and all races will be included

Exclusion Criteria

  • Women who are breastfeeding or pregnant
  • Individuals with medical conditions unsuitable for MR scanning
  • Individuals reporting a history of epilepsy or seizures
  • Individuals reporting an allergy to cycloserine
  • Individuals diagnosed with asthma or who report previous anaphylactic reaction to insect stings/bites, medication, food, or other material and/or event
  • Individuals reporting present or past diagnosis of a developmental disorder, neurological disorder, or head injury *Individuals found to have Axis I psychopathology as defined by the DSM-IV (other than spider phobia)
  • Individuals currently taking any psychotropic medication
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00591825). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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