Costs of Lost Productive Time Among Korean Workers With Panic Disorder and Effect of Treatment With Paroxetine Controlled Release

The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2007 by Inje University.
Recruitment status was  Recruiting
Sponsor:
Collaborator:
GlaxoSmithKline
Information provided by:
Inje University
ClinicalTrials.gov Identifier:
NCT00492414
First received: June 26, 2007
Last updated: August 7, 2007
Last verified: March 2007

June 26, 2007
August 7, 2007
 
 
 
 
Complete list of historical versions of study NCT00492414 on ClinicalTrials.gov Archive Site
 
 
 
 
 
Costs of Lost Productive Time Among Korean Workers With Panic Disorder and Effect of Treatment With Paroxetine Controlled Release
 

Panic disorder(PD)is a disabling psychiatric condition associated with significant impairment in psychosocial, occupational functioning and quality of life, as mentioned by mogotsi et al. So, most patients with panic disorder suffers from the consequences of the impairment in occupational function. This impairment is not only individual problem, but also social one. Since productivity is very important item required to employees, lost productive time among workers with psychiatric illness should be reduced by the proper management. But few data were reported in this field by now.

 
Interventional
Phase 4
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Health Services Research
Panic Disorder
Drug: Paroxetine CR
 
 

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
 
 
 

Inclusion Criteria:

  1. Male or female outpatients aged 20-50 years
  2. In female, is eligible to enter this study if she is if

    • Non-childbearing potential(note:women who are 6 months post-menopausal are not considered women of child-bearing potential)
    • child-bearing potential, has a negative urine dipstick pregnancy test, and is practicing a clinically acceptable method of contraception such as oral contraception, surgical sterilization, I.U.D.,systemic contraception, or double barrier contraception(any two of diaphragm/spermicidal foar/condom)
  3. Subject currently meets the diagnosis for PD according to korean version of Anxiety Disorder Interview Schedule for DSM-IV(ADIS-IV) through a comprehensive psychiatric evaluation and not being treated currently.
  4. Subject must have the ability to comprehend the key components of the consent form and provide informed consent.

Exclusion Criteria:

  1. Subject who has a history of any other major medical or psychiatric illnesses except PD or PD with major depressive disorder.
  2. Subject who retired or left his job or who plan to retire within two years.
  3. is a current homicidal or suicidal risk in the investigator's judgement.
  4. is currently pregnant, lactating or planning to become pregnant within the next 3 months
  5. is currently participating in any other clinical trial or taking any non-approved or experimental medication.
Both
20 Years to 50 Years
 
Contact: Eun-Joo Jung +82-2-2270-0940 menfipro@naver.com
Korea, Republic of
 
NCT00492414
COL110010
 
 
Inje University
GlaxoSmithKline
Principal Investigator: Jong-Min Woo, Master Seoul Paik Hospital, Inje University
Inje University
March 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP