Risperidone vs. Paroxetine for Panic Attacks
|First Submitted Date ICMJE||September 13, 2005|
|First Posted Date ICMJE||September 21, 2005|
|Last Update Posted Date||October 22, 2012|
|Start Date ICMJE||January 2003|
|Primary Completion Date||July 2005 (Final data collection date for primary outcome measure)|
|Current Primary Outcome Measures ICMJE||Not Provided|
|Original Primary Outcome Measures ICMJE||Not Provided|
|Change History||Complete list of historical versions of study NCT00206765 on ClinicalTrials.gov Archive Site|
|Current Secondary Outcome Measures ICMJE||Not Provided|
|Original Secondary Outcome Measures ICMJE||Not Provided|
|Current Other Outcome Measures ICMJE||Not Provided|
|Original Other Outcome Measures ICMJE||Not Provided|
|Brief Title ICMJE||Risperidone vs. Paroxetine for Panic Attacks|
|Official Title ICMJE||A Single-blind Trial of Risperidone vs. Paroxetine for Treatment of Panic Attacks|
|Brief Summary||We are comparing the efficacy of Risperidone versus Paroxetine in the treatment of panic symptoms. The study hypothesis is that Risperidone will be a superior medicine for treating panic.|
Risperidone is an atypical antipsychotic drug that acts as an antagonist at 5-HT2A/2C and D2 receptors (Chouignard et al, 1993; Marder & Meibach, 1994). In its serotonergic activity, risperidone resembles both the atypical antidepressant and 5HT2-antagonist nefazodone (Bakish et al, 1993) and a 5HT2-antagonist ritanserine (Lima & Moncrieff, 2000; Preskorn 1995). Nefazodone treats anxiety symptoms and induces less agitation than other reuptake blockers (Fawcett et al, 1995) while ritanserin shows effectiveness in treatment of dysthymia in clinical trials. Moreover, risperidone increases release of dopamine and norepinephrine in the prefrontal cortex (Zhang et al, 2000), an activity that in other pharmacological agents is associated with their antidepressant, anxiolytic, and antipanic properties (Thase, 2002).
Therefore, risperidone has a potential to be effective for treatment of either Generalized Anxiety Disorder, or Panic Disorder, or Major Depressive Disorder with Panic Attacks (DSM-IV, 1994) as a single agent. Moreover, due to its D2 and 5-HT2A/2C antagonism and proven antipsychotic efficacy, the drug could be uniquely effective for severe panic attacks with psychotic features or para-psychotic features (Galynker et al, 1996). Consistent with this supposition, Marder et al (1997) reported that in patients with schizophrenia, risperidone produced significantly greater improvements than haloperidol in PANSS scores measuring anxiety and depression.
Our clinical experience with over 50 patients with panic attacks showed that low dose risperidone, similar to lorazepam, reduced or eliminated anxiety and panic, often after the first dose. Risperidone was most effective for patients experiencing obsessive, intrusive, anxiety-inducing thoughts. In contrast to lorazepam, risperidone treatment did not result in building of tolerance to the drug or disinhibition. We did not observe extrapyramidal side effects in patients treated with risperidone for panic attacks. Thus, our preliminary clinical data indicate that due to its efficacy, quick onset of action, absence of addictive potential, and lack of side effects, risperidone could be superior to both benzodiazepines and SSRIs for treatment of panic attacks, particularly for severe panic attacks. Moreover, risperidone has a potential to be the first line drug for treatment of these symptoms.
Consequently, at present, a clinical study of risperidone for treatment of panic attacks is indicated and is of great potential value. We are therefore proposing an exploratory open label single-blind trial of risperidone in vs. paroxetine for treatment of panic attacks.
Objective One. To compare the efficacy of risperidone to that of paroxetine in treatment of panic attacks in patients with Panic Disorder and with Major Depressive Disorder with Panic attacks.
Hypothesis One: Risperidone and will be more efficacious in treatment of panic symptoms in both patient groups. Some patients will improve within 24 hrs.
Objective Two. To compare the side effect profile of risperidone vs. paroxetine in treatment of panic attacks.
Hypothesis Two: Risperidone, compared to paroxetine, will cause less sexual side effects, anxiety, and restlessness. There will be no difference in extrapyramidal side effects between the paroxetine and the risperidone groups.
Objective Three. To compare response rates of risperidone vs. paroxetine in treatment of panic attacks.
Hypothesis Three: Patients with panic attacks will respond significantly faster to risperidone that to paroxetine.
Objective Four. To examine demographic and clinical predictors of robust response to risperidone treatment using appropriate statistical analysis of individual scales items and treatment response rates.
Hypothesis Four: The subgroup patients with panic attacks who will have high scores on items reflecting somatic anxiety, and ruminative intrusive thinking, and those with nocturnal panic attacks will show better response to risperidone therapy than patients with low scores on those items.
If study hypotheses are confirmed, future research could include a randomized, double blind fixed dose study of risperidone as the sole agent for treatment of panic disorder and Phase IV trials aimed to determine the effectiveness of 0.125 mg and 0.0675 mg dose of risperidone for treatment of anxiety and panic attacks.
The patient population will consist of psychiatric outpatients who meet criteria for the DSM-IV diagnosis of Major Depressive Disorder with Panic Attacks or Panic Disorder. The subjects will be recruited from the Center for Treatment of Affective Disorders and from the Anxiety and Trauma Center in the Department of Psychiatry at the Beth Israel Medical center that provide care to 900 patients. At present, the patient ethnic and racial mix is 50% Hispanic, 15% African American, 32.5% Caucasian and 2.5% Asian. The gender distribution is approximately 33% male and 67 % female. The outpatient payer mix is 20 % Medicare, 74 % Medicaid and 6% combined. Of those patients, approximately 40% (360) manifest panic attacks. Based on our previous experience with recruitment for research studies, we expect that 10-12% of patients (36-42) meeting diagnostic criteria will also meet the inclusion and exclusion criteria, will sign the inform consent and will participate in the study. We expect to recruit 40 patients per year and to complete the study in 3 years.
Study Design and Drug Regimens
The study will be an 8-week parallel comparison (with a blinded rater) of risperidone and paroxetine for treatment of three groups of patients with panic attacks. Each group will consist of 30 subjects.
After signing an informed consent, the subjects will be randomly assigned in the open manner to treatment with risperidone or paroxetine alone.
Arm 1: Treatment with risperidone will be flexible-dose and will be initiated at 0.25 mg po qhs. For the subjects who did not achieve a remission of panic symptoms, the dose will be increased to 0.5 mg po qhs on day 3. For subjects who experienced morning sedation, the dose will be decreased to 0.125-mg po qhs on day 3.
Arm 2: Treatment with Paroxetine will be flexible-dose and will be initiated at 10-mg po qhs. For subjects who experienced morning sedation, the dose will be decreased to 5-mg po qhs on day 3. For the subjects who did not achieve a remission of panic symptoms, the dose will be increased to 20-mg po qhs. For the subjects who did not achieve a remission of panic symptoms, the dose will be increased to 40-mg po qhs as needed.
Arm 3: Treatment with Paroxetine on a fixed dose schedule will be initiated at 10 mg po qhs on day 1. On day 3 it will be increased to 20 mg po qhs. On day 7 it will be increased to 30 mg po qhs. Most patients respond to an average therapeutic dose of 30 mg of paroxetine.. This will ensure that a subgroup of subjects will receive optimum therapeutic dose of Paroxetine and also aid to titrate Paroxetine equivalent dose of Risperidone.
Patients randomized on any of the above arms, and not responding or having side effects will be taken off the study and referred for regular psychiatric treatment.
The subjects receiving fixed dose antidepressants or mood stabilizers prior to their enrollment in the study will be continued on these medications throughout the study. No dose adjustment of antidepressants or mood stabilizers will be allowed. At the end of study, participants can choose to continue their study medications under the care of one of study physicians or one of the other psychiatrists at Psychiatric outpatients service for adults Beth Israel Medical Center 16 Street at First Avenue, 2 Bernstein. Those wishing to stop the study medications at the end of the study will be able to do so under the supervision of one of the study physicians. Paroxetine will be tapered over a two-week period to avoid SSRI withdrawal. Risperidone will be stopped abruptly since no withdrawal symptoms have been reported in the literature making risperidone taper unnecessary.
Assessments to evaluate mood improvement will be performed by a rater blinded to medication status on a daily basis for the first three days and every other day for the first two weeks. The assessments (please see Appendix 1 for the assessment battery) will continue weekly for the rest of the study.
All study participants' will provided with psychiatric treatment, free of charge, at our clinic, for one month following the end of the study. At the end of one-month period, we will assist you in finding further psychiatric care. Travel expenses will be reimbursed for the subjects participating in the study.
We will calculate Pearson Product Moment correlation coefficients (r) for each of the treatment outcome variable groups. This will enable us to determine the degree of association between treatment and outcome. More importantly, we can interpret (r) with the Binomial Effect Size Display (BESD) (Rosenthal, 1991). The BESD will enable us to estimate a clinically meaningful improvement rate and to estimate the number of people that would improve as a result of treatment.
Power Analysis and Precision Analysis
As stated above, our measure of effect size will be the Pearson Product Moment correlation coefficient (r). For this study we chose an effect size of r = .50 as the smallest effect size that would be clinically meaningful, and then calculated that we would need a sample size of 26, to obtain power of 81%, and a 95.0% confidence interval (r = .13 to r = .75) that would not include zero. (Rosenthal, 1991).
|Study Type ICMJE||Interventional|
|Study Phase||Phase 2|
|Study Design ICMJE||Allocation: Randomized
Intervention Model: Parallel Assignment
Primary Purpose: Treatment
|Study Arms||Not Provided|
|Publications *||Not Provided|
* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
|Recruitment Status ICMJE||Terminated|
|Estimated Enrollment ICMJE||90|
|Completion Date||July 2005|
|Primary Completion Date||July 2005 (Final data collection date for primary outcome measure)|
|Eligibility Criteria ICMJE||
|Ages||21 Years to 55 Years (Adult)|
|Accepts Healthy Volunteers||No|
|Contacts ICMJE||Contact information is only displayed when the study is recruiting subjects|
|Listed Location Countries ICMJE||United States|
|Removed Location Countries|
|NCT Number ICMJE||NCT00206765|
|Other Study ID Numbers ICMJE||082-02|
|Has Data Monitoring Committee||Not Provided|
|U.S. FDA-regulated Product||Not Provided|
|IPD Sharing Statement||Not Provided|
|Responsible Party||Beth Israel Medical Center|
|Study Sponsor ICMJE||Beth Israel Medical Center|
|Collaborators ICMJE||Not Provided|
|PRS Account||Beth Israel Medical Center|
|Verification Date||October 2012|
ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP