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Vestibular Dysfunction In Adult Patients With Panic Disorder With or Without Agoraphobia

This study has been completed.

Sponsors and Collaborators: National Center for Research Resources (NCRR)
University of Pittsburgh
Information provided by: National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier: NCT00004367
  Purpose

OBJECTIVES: I. Determine whether the prevalence of abnormalities on clinical vestibular (balance) tests is higher in panic disorder with agoraphobia than in uncomplicated panic disorder and nonpanic anxiety disorder.

II. Determine whether the prevalence of abnormalities on audiological tests of cochlear or brainstem function is elevated in panic disorder without agoraphobia or nonpanic anxiety disorder.

III. Determine whether symptom patterns can be identified that are indicative of vestibular abnormalities in panic disorder.

IV. Determine whether vestibular dysfunction can be induced by psychosomatic mechanisms.


Condition Intervention
Anxiety Disorder
Panic Disorder
Procedure: Clinical vestibular tests

MedlinePlus related topics:   Anxiety    Panic Disorder   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Diagnostic

Further study details as provided by National Center for Research Resources (NCRR):

Estimated Enrollment:   165
Study Start Date:   May 2000

Detailed Description:

PROTOCOL OUTLINE: Patients are stratified by otoneurological function (panic disorder without agoraphobia, panic disorder with agoraphobia, anxiety disorder without panic or agoraphobia-like avoidance, and normal controls).

Patients undergo a psychiatric interview and a structured interview focused on anxiety disorders. Physical evaluation is completed.

A vestibular evaluation consisting of posturography, rotational testing, and ocular motor screening battery, and positional and caloric testing is completed on all patients. Patients then complete an audiological test battery consisting of basic audiological analysis, speech recognition scores, immittance testing, brainstem evoked response, and determination of binaural masking level differences.

Control patients also complete a hyperventilation-rotational test.

  Eligibility
Ages Eligible for Study:   18 Years to 55 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes

Criteria

PROTOCOL ENTRY CRITERIA:

--Disease Characteristics-- Diagnostically proven panic disorders with or without moderate or severe agoraphobia and anxiety disorders without panic or agoraphobia Panic disorder may be accompanied by a secondary Axis 1 diagnosis of another disorder, such as depression, generalized anxiety disorder, or dependent, histrionic, or compulsive personality disorder --Prior/Concurrent Therapy-- Surgery: No prior ear surgery Other: No concurrent medication for medical or psychiatric conditions At least 2 weeks since prior medication No ototoxic drug intake --Patient Characteristics-- No medical disorders At least 2 weeks since prior upper respiratory tract infection and recovered No history of migraine No head trauma No scoliosis No alcoholism No drug abuse No family history of schizophrenia

  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00004367

Locations
United States, Pennsylvania
University of Pittsburgh    
      Pittsburgh, Pennsylvania, United States, 15260

Sponsors and Collaborators

Investigators
Study Chair:     Rolf G. Jacob     University of Pittsburgh    
  More Information


Study ID Numbers:   199/11945, UPITTS-9504279605
First Received:   October 18, 1999
Last Updated:   June 23, 2005
ClinicalTrials.gov Identifier:   NCT00004367
Health Authority:   United States: Federal Government

Keywords provided by National Center for Research Resources (NCRR):
anxiety disorder  
disease-related problem/condition  
neurologic and psychiatric disorders  
panic disorder  
rare disease  

Study placed in the following topic categories:
Panic Disorder
Anxiety Disorders
Mental Disorders
Rare Diseases
Agoraphobia

Additional relevant MeSH terms:
Pathologic Processes
Disease

ClinicalTrials.gov processed this record on November 30, 2008




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