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Long Term Treatment of Panic Disorder With Clonazepam or Paroxetine (LTTPANIC)

Primary Purpose

Panic Disorder, Agoraphobia

Status
Completed
Phase
Phase 4
Locations
Brazil
Study Type
Interventional
Intervention
Clonazepam
Paroxetine
Sponsored by
Universidade Federal do Rio de Janeiro
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Panic Disorder focused on measuring panic disorder, agoraphobia, clonazepam, paroxetine

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Diagnosis of panic disorder, with or without agoraphobia according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, text revision (DSM-IV-TR) criteria, as determined by a structured clinical interview.
  • At least two panic attacks in the week preceding their inclusion in the study.

Exclusion Criteria:

  • Patients unable or unwilling to provide written informed consent.
  • Did not complete all the evaluations before study initiation.
  • Had comorbidities that could affect clinical evaluation including drug abuse, neurological disorders, or severe personality disorder.

Sites / Locations

  • Instituto de Psiquiatria da Universidade Federal do Rio de Janeiro

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Clonazepam

Paroxetine

Arm Description

Treatment with clonazepam

Treatment with paroxetine

Outcomes

Primary Outcome Measures

Clinical Global Impression Severity scores at 8 weeks

Secondary Outcome Measures

Clinical Global Impression Severity scores at 36 months
Clinical Global Impression Severity scores at 4 years
Clinical Global Impression Severity scores at 9 years
Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 8 weeks
Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 36 months

Full Information

First Posted
July 21, 2016
Last Updated
July 28, 2016
Sponsor
Universidade Federal do Rio de Janeiro
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico
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1. Study Identification

Unique Protocol Identification Number
NCT02852577
Brief Title
Long Term Treatment of Panic Disorder With Clonazepam or Paroxetine
Acronym
LTTPANIC
Official Title
Long-term, Open, Naturalistic, Randomized Clinical Trial With Clonazepam and Paroxetine in Panic Disorder With or Without Agoraphobia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2016
Overall Recruitment Status
Completed
Study Start Date
January 2000 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Federal do Rio de Janeiro
Collaborators
Conselho Nacional de Desenvolvimento Científico e Tecnológico

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study was to determine whether clonazepam and paroxetine are effective in the treatment of panic disorder. Efficacy was evaluated in short-term, long-term and post-treatment.
Detailed Description
The current study consisted of three steps. The first step was a naturalistic, prospective, randomized, open clinical trial with clonazepam and paroxetine. Subjects received either flexible dose clonazepam (0.5 - 2 mg/day) or paroxetine (10 - 40 mg/day), in monotherapy for eight weeks. In the second step, those who responded to monotherapy in the short-term study continued with the same drug and dose. Partial responders or non-responders were invited to receive combined pharmacological treatment with clonazepam and paroxetine. Patients received the maximum tolerated doses of clonazepam and paroxetine. The doses were flexible, ranging from 0.5 to 2 mg/day for clonazepam and from 10 to 40 mg/day of paroxetine. All patients were treated for 34 months in the second step. Patients who completed the second step and were in remission were included in the third step. For a period of four months all medications were tapered off. These patients were followed for 6 years with evaluations once a year. Those who relapsed were treated on a naturalistic basis, with drugs or psychotherapy. This study was conducted in accordance with the ethical principles established by the Declaration of Helsinki and the Brazilian National Ethics Committee (Conselho Nacional de Ética em Pesquisa - CONEP) guidelines. The local Ethics Committee approved the study protocol. Written informed consent was obtained from all patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Panic Disorder, Agoraphobia
Keywords
panic disorder, agoraphobia, clonazepam, paroxetine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Clonazepam
Arm Type
Active Comparator
Arm Description
Treatment with clonazepam
Arm Title
Paroxetine
Arm Type
Active Comparator
Arm Description
Treatment with paroxetine
Intervention Type
Drug
Intervention Name(s)
Clonazepam
Intervention Description
Administration of clonazepam once a day, flexible dose (0.5 - 2 mg/day), for 36 months. If no remission after 8 weeks augmentation with paroxetine once a day, flexible dose (10 - 40 mg/day), for 34 months.
Intervention Type
Drug
Intervention Name(s)
Paroxetine
Intervention Description
Administration of paroxetine once a day, flexible dose (10 - 40 mg/day), for 36 months. If no remission after 8 weeks augmentation with clonazepam once a day, flexible dose (0.5 - 2 mg/day), for 34 months.
Primary Outcome Measure Information:
Title
Clinical Global Impression Severity scores at 8 weeks
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Clinical Global Impression Severity scores at 36 months
Time Frame
36 months
Title
Clinical Global Impression Severity scores at 4 years
Time Frame
4 years
Title
Clinical Global Impression Severity scores at 9 years
Time Frame
9 years
Title
Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 8 weeks
Time Frame
Baseline, 8 weeks
Title
Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 36 months
Time Frame
Baseline, 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosis of panic disorder, with or without agoraphobia according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, text revision (DSM-IV-TR) criteria, as determined by a structured clinical interview. At least two panic attacks in the week preceding their inclusion in the study. Exclusion Criteria: Patients unable or unwilling to provide written informed consent. Did not complete all the evaluations before study initiation. Had comorbidities that could affect clinical evaluation including drug abuse, neurological disorders, or severe personality disorder.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rafael C Freire, MD, PhD
Organizational Affiliation
Universidade Federal do Rio de Janeiro
Official's Role
Principal Investigator
Facility Information:
Facility Name
Instituto de Psiquiatria da Universidade Federal do Rio de Janeiro
City
Rio de Janeiro
ZIP/Postal Code
22290140
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21344132
Citation
Nardi AE, Valenca AM, Freire RC, Mochcovitch MD, Amrein R, Sardinha A, Levitan MN, Nascimento I, de-Melo-Neto VL, King AL, de O E Silva AC, Veras AB, Dias GP, Soares-Filho GL, da Costa RT, Mezzasalma MA, de Carvalho MR, de Cerqueira AC, Hallak JE, Crippa JA, Versiani M. Psychopharmacotherapy of panic disorder: 8-week randomized trial with clonazepam and paroxetine. Braz J Med Biol Res. 2011 Apr;44(4):366-73. doi: 10.1590/s0100-879x2011007500020. Epub 2011 Feb 18.
Results Reference
result
PubMed Identifier
21364347
Citation
Nardi AE, Valenca AM, Freire RC, Amrein R, Sardinha A, Levitan MN, Nascimento I, de-Melo-Neto VL, King AL, de O e Silva AC, Veras AB, Dias GP, Soares-Filho GL, da Costa RT, Mezzasalma MA, de Carvalho MR, de Cerqueira AC, Hallak JE, Crippa JA, Versiani M. Randomized, open naturalistic, acute treatment of panic disorder with clonazepam or paroxetine. J Clin Psychopharmacol. 2011 Apr;31(2):259-61. doi: 10.1097/JCP.0b013e318210b4ee. No abstract available.
Results Reference
result
PubMed Identifier
22198456
Citation
Nardi AE, Freire RC, Mochcovitch MD, Amrein R, Levitan MN, King AL, Valenca AM, Veras AB, Paes F, Sardinha A, Nascimento I, de-Melo-Neto VL, Dias GP, E Silva AC, Soares-Filho GL, da Costa RT, Mezzasalma MA, de Carvalho MR, de Cerqueira AC, Hallak JE, Crippa JA, Versiani M. A randomized, naturalistic, parallel-group study for the long-term treatment of panic disorder with clonazepam or paroxetine. J Clin Psychopharmacol. 2012 Feb;32(1):120-6. doi: 10.1097/JCP.0b013e31823fe4bd. Erratum In: J Clin Psychopharmacol. 2012 Apr;32(2):206.
Results Reference
result

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Long Term Treatment of Panic Disorder With Clonazepam or Paroxetine

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