Status:
COMPLETED
The Effect of an Additional Bolus Application in Patients With Intrathecal Opiate Administration - a Pilot Study
Lead Sponsor:
Swiss Paraplegic Research, Nottwil
Conditions:
Chronic Pain Syndrome
Eligibility:
All Genders
18-99 years
Brief Summary
An additional, intermittent bolus application in patients with intrathecal opiate administration for chronic pain syndrome may have a positive effect on the effectiveness of the treatment. Thus, the e...
Eligibility Criteria
Inclusion
- chronic pain syndrome
- intrathecal opiate pump
- signed informed consent
Exclusion
- younger than 18 years
- other (than opiate) intrathecal drug administration
- discontent with intrathecal opiate therapy
Key Trial Info
Start Date :
February 1 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
July 1 2014
Estimated Enrollment :
10 Patients enrolled
Trial Details
Trial ID
NCT02197741
Start Date
February 1 2012
End Date
July 1 2014
Last Update
November 22 2016
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