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Observational Study on the Patients With Pain Medications

Completed
Conditions
Pain
Interventions
Other: Observational pain control study
Registration Number
NCT00771212
Lead Sponsor
Johnson & Johnson Taiwan Ltd
Brief Summary

The purpose of this study is to describe the use of pain treatments in Taiwan, the demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment.

Detailed Description

This is a Phase IV, multi-center, observational study to describe the use of pain treatments, the demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment. The study is conducted in an effort to understand the status of pain control in Taiwan. Currently in Taiwan, there is no approved documentation showing the most effective standard medication for treatment of patients in pain. Observational study with no study medication administered.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
2636
Inclusion Criteria
  • Outpatients only
  • Patients must have pain, previously treated with and without medication and have a VAS (Visual analogue scale) score recorded at the enrolment time
  • Patient must have a VAS score >4
Exclusion Criteria
  • Patients who are receiving any investigational drug during the study
  • Patients with known or suspected psychotic disease or mental retardation.

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
001Observational pain control study-
Primary Outcome Measures
NameTimeMethod
To describe effective use of pain medications, describe demographics, clinical characteristics of patients requiring pain treatments, current treatments, outcomes of treatments and the reasons for changing pain medication during treatment in Taiwan60 days
Secondary Outcome Measures
NameTimeMethod
Pain Relief Rating Scale60 days
Global Assessments (Patient/Investigator)60 days
Sleeping quality Assessment60 days
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