NCT03016364UnknownPhase 1
Application Software in Dosage Adjustment for Advanced Cancer Patients With Pain
Cancer Institute and Hospital, Chinese Academy of Medical Sciences1 site in 1 country200 target enrollmentStarted: January 1, 2017Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Phase 1
- Enrollment
- 200
- Locations
- 1
- Primary Endpoint
- Numerical Pain Rating Scale
Study Overview
Brief Summary
The purpose of this trial is to determine whether Application (APP) would help clinical doctors to adjust the dose of Oxycodone Hydrochloride Prolonged-release Tablets in advanced patients with cancer pain.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Intervention Model
- Single Group
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 70 Years (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •a histologically confirmed diagnosis of Cancer or Sarcoma
- •advanced patients with severe cancer pain(score >3)
- •having used or expected to use the Oxycodone Hydrochloride Prolonged-release Tablets
Exclusion Criteria
- •allergic to Oxycodone Hydrochloride Prolonged-release Tablets, or other reasons (determined by clinical doctors) unable to use the Opioids
Arms & Interventions
APP in dosage adjustment
Experimental
Through the guidance of APP software, clinical doctors try to adjust the dose of Oxycodone Hydrochloride Prolonged-release Tablets for advanced patient's with cancer pain.
Intervention: APP software (Device)
Outcomes
Primary Outcomes
Numerical Pain Rating Scale
Time Frame: upto 8 months
Secondary Outcomes
No secondary outcomes reported
Investigators
Peng Liu
Attending Physician
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Study Sites (1)
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