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OpenTrials
Completed

NCT Number: NCT02852577

Long Term Treatment of Panic Disorder With Clonazepam or Paroxetine

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.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Instituto de Psiquiatria da Universidade Federal do Rio de Janeiro

Rio de Janeiro, 22290140, Brazil

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Clonazepam

Drug

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.

paroxetine

Drug

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 outcomes

  1. Clinical Global Impression Severity scores at 8 weeks

    Time frame: 8 weeks

Secondary outcomes

  1. Clinical Global Impression Severity scores at 36 months

    Time frame: 36 months

  2. Clinical Global Impression Severity scores at 4 years

    Time frame: 4 years

  3. Clinical Global Impression Severity scores at 9 years

    Time frame: 9 years

  4. Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 8 weeks

    Time frame: Baseline, 8 weeks

  5. Change from baseline of Clinical Global Impression Severity (CGI-S) scale scores at 36 months

    Time frame: Baseline, 36 months

Sponsors and collaborators

Lead sponsor

Universidade Federal do Rio de Janeiro

Other

Collaborators

  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

Registry information

Official study title

Long-term, Open, Naturalistic, Randomized Clinical Trial With Clonazepam and Paroxetine in Panic Disorder With or Without Agoraphobia

Acronym: LTTPANIC

Important dates

Study start
2000
Primary completion
2012
Study completion
2012
First posted
Aug 2, 2016
Registry last updated
Aug 2, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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