Study of Escitalopram in the Treatment of Specific Phobia

NCT00121069 · Status: COMPLETED · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2005-07-21

No results posted yet for this study

Summary

This pilot study is designed to assess the efficacy of escitalopram in the treatment of specific phobia in adult outpatients.

Conditions

  • Phobic Disorders

Interventions

DRUG

Escitalopram

Sponsors & Collaborators

  • Forest Laboratories

    collaborator INDUSTRY
  • Connor, Kathryn M., M.D.

    lead INDIV

Principal Investigators

  • Kathryn M. Connor, M.D. · Duke University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2002-09-30
Completion
2004-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00121069 on ClinicalTrials.gov