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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03016364
Other study ID # CFH2016-3-4025
Secondary ID
Status Recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date January 2017
Est. completion date December 2019

Study information

Verified date January 2019
Source Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Contact Peng Liu, MD
Phone 8610-87788405
Email 13910216310@163.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Device:
APP software
A software used to by physicians to adjust the dose of Oxycodone Hydrochloride Prolonged-release Tablets for advanced patient's with cancer pain

Locations

Country Name City State
China Cancer Hospital, Chinese Academy of Medical Sciences Beijing Beijing

Sponsors (1)

Lead Sponsor Collaborator
Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Numerical Pain Rating Scale upto 8 months
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