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Clinical Trials/NCT01718821
NCT01718821
Completed
Not Applicable

Assessments on Current Pain Managements in Upper Gastrointestinal Cancer Patients

National Cheng Kung University1 site in 1 country50 target enrollmentSeptember 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
National Cheng Kung University
Enrollment
50
Locations
1
Primary Endpoint
Pain, assessed by BPI-SF.
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Pain is one of the most common symptoms associated with cancer. The approach to pain management compresses routine pain assessments, utilizes both pharmacologic and nonpharmacologic interventions, and requires ongoing reevaluation of the patient. Cancer pain can be well controlled in the vast majority of patients if the algorithms of pain control are systematically applied, carefully monitored, and tailored to the needs of the individual patient.This study is aimed to assess the current pain managements in upper gastrointestinal cancer patients in Taiwan. The effects of neuropathic pain and depression on the enrolled patients would also be assessed.

Registry
clinicaltrials.gov
Start Date
September 2012
End Date
September 2014
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hsu-chih Chien

Doctoral student

National Cheng Kung University

Eligibility Criteria

Inclusion Criteria

  • with a diagnose of advanced upper GI cancer based on pathology or imaging studies
  • could report pain intensities and answer questionnaires by him/herself

Exclusion Criteria

  • with major neurologic or psychiatric diseases
  • could not report pain intensities and answer questionnaires by him/herself

Outcomes

Primary Outcomes

Pain, assessed by BPI-SF.

Time Frame: Assessed at enrolled date (Day 1)

Pain intensities of participants would be assessed by BPI-SF at D1.

Changes in pain, assessed by BPI-SF.

Time Frame: Baseline and 1 month.

Changes in pain intensities of participants would be assessed by BPI-SF. The changes in pain would be assessed again after 1 month when participants have outpatient visits or during their admission. An expected following duration average of would be 4 weeks.

Secondary Outcomes

  • Depression, assessed by two stem questions.(Assessed at enrolled date (Day 1))
  • Changes in depression, assessed by two stem questions.(Baseline and 1 month.)
  • Quality of life, assessed by EROTC QLQ C30.(Day 1)
  • Neuropathic pain, assessed by DN4 questions.(Day 1)
  • Changes in quality of life. Quality of life, assessed by EROTC QLQ C30.(Baseline and 1 month.)
  • Changes in neuropathic pain. Neuropathic pain, assessed by DN4 questions.(Baseline and 1 month.)

Study Sites (1)

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