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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00000389
Other study ID # N01MH60005
Secondary ID N01MH60016DSIR C
Status Completed
Phase Phase 3
First received November 2, 1999
Last updated June 13, 2007
Start date October 1996
Est. completion date November 1999

Study information

Verified date November 2005
Source National Institute of Mental Health (NIMH)
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if it is effective to treat children with anxiety disorders with fluvoxamine.

Fluvoxamine has been successfully used to treat obsessive-compulsive disorder (OCD) in adults and children. Anxiety disorders other than OCD, such as generalized anxiety disorder, social phobia, or separation anxiety, are very common in youth and are not always responsive to behavioral therapies alone. These disorders may respond to fluvoxamine.

A child will be evaluated for 3 weeks before he/she is assigned randomly (like tossing a coin) to receive either fluvoxamine or an inactive placebo for 8 weeks. After this double-blind phase (neither the child/parents nor the doctor know which treatment is being given), the child will have the option of continuing treatment during a 4-month open-label extension period (both the child/parents and the doctor know which the child is receiving).

A child may be eligible for this study if he/she:

Is 6 to 17 years old and has been diagnosed with an anxiety disorder (i.e., generalized anxiety disorder, social phobia, or separation anxiety).


Description:

To evaluate fluvoxamine in the treatment of children and adolescents with anxiety disorders.

Fluvoxamine is a serotonin reuptake inhibitor that is FDA-approved for the treatment of obsessive-compulsive disorder (OCD) in adults and children. Anxiety disorders other than OCD are very common in youth and are not always responsive to psychosocial therapies. Fluvoxamine is an alternative treatment.

After a 3-week period of evaluation, patients meeting study entry criteria are randomized to receive either fluvoxamine or placebo for 8 weeks. After this double-blind phase, patients can enter a 4-month open-label extension.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date November 1999
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 6 Years to 17 Years
Eligibility - Patients must have: DSM -IV diagnosis of generalized anxiety disorder, social phobia, or separation anxiety.

Study Design

Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
Fluvoxamine


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Institute of Mental Health (NIMH)

References & Publications (2)

Coyle JT. Drug treatment of anxiety disorders in children. N Engl J Med. 2001 Apr 26;344(17):1326-7. — View Citation

Fluvoxamine for the treatment of anxiety disorders in children and adolescents. The Research Unit on Pediatric Psychopharmacology Anxiety Study Group. N Engl J Med. 2001 Apr 26;344(17):1279-85. — View Citation

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