A Study of Sertraline and Early Alprazolam XR Administration Versus Sertraline Only in Panic Disorder Patients

Indiana University School of Medicine

Status and phase

Completed

Phase 4

Conditions

Panic Disorder

Treatments

Drug: Sertraline and Alprazolam XR

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00198094

IU 1003

0311-34

Details and patient eligibility

About

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.

Enrollment

150 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.