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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00198094
Other study ID # 0311-34
Secondary ID IU 1003
Status Completed
Phase Phase 4
First received September 12, 2005
Last updated October 19, 2007
Start date December 2003
Est. completion date September 2007

Study information

Verified date October 2007
Source Indiana University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary objective for the study is to test the hypothesis that sertraline plus alprazolam XR will result in superior early stabilization of primary care PD patients versus sertraline/placebo over a 12-week treatment period. The secondary objectives of the study are a) to assess withdrawal symptoms during alprazolam XR taper (weeks 5-7 of the 12-week trial) and after discontinuation, b) to compare physical health outcomes, medical services utilization, and cost-effectiveness of the two study interventions across the 12-week treatment period and subsequent three month maintenance treatment with sertraline alone, and c) to assess whether early co-administration of sertraline/ alprazolam XR will result in greater maintenance of treatment response than sertraline/placebo over the three months following the 12 week acute treatment program.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date September 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Subjects will include men and women over the age of eighteen;

- the ability to give written informed consent;

- current principal or co-principal psychiatric diagnosis of panic disorder with or without agoraphobia based on DSM-IV criteria (American Psychiatric Association, 1994);

- willing to use an effective means of contraception;

- free of psychoactive medications for at least 2 weeks prior to study enrollment;

- not actively be suicidal.

Exclusion Criteria:

- actively suicidal;

- medical conditions for which either sertraline or alprazolam XR would be contraindicated;

- recent six month history of substance or alcohol abuse;

- history or presence of psychotic or bipolar disorder;

- women who are pregnant or breastfeeding;

- history or presence of a seizure disorder or a known history of more than one childhood febrile seizure;

- presence of a personality disorder severe enough to compromise the investigator's ability to evaluate the efficacy and safety of the study medication;

- concomitant therapy with other psychotropic medication(s);

- clinically significant abnormality during physical examination, vital signs, EKG, urine drug screen, or laboratory tests at the screen visit.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Sertraline and Alprazolam XR


Locations

Country Name City State
United States University Hospital Outpatient Center, Psychiatry Indianapolis Indiana
United States University of Pennsylvania, Mood and Anxiety Disorders Section Philadelphia Pennsylvania
United States University of South Florida, Department of Psychiatry and Behavioral Medicine Tampa Florida

Sponsors (4)

Lead Sponsor Collaborator
Indiana University School of Medicine Pfizer, University of Pennsylvania, University of South Florida

Country where clinical trial is conducted

United States, 

References & Publications (1)

A randomized double-blind comparison of sertraline with early alprazolam XR Co-administration vs. sertraline/placebo for panic disorder. Goddard AW, Ball SG, Hastings AK, Shekhar A, Rickels K, Rynn M, Janavs J, Sheehan DV. BIOLOGICAL PSYCHIATRY 57 (8): 62

Outcome

Type Measure Description Time frame Safety issue
Primary Panic symptoms scale score
Primary CGI-I
Primary CGI-S
Secondary Sheehan Disability Scale
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