Status:
COMPLETED
PANDA-Regional Feasibility Study of a Smartphone Pain Management Application
Lead Sponsor:
University of British Columbia
Conditions:
Postoperative Pain
Anesthesia, Conduction
Eligibility:
All Genders
19-75 years
Phase:
NA
Brief Summary
Despite the numerous benefits of peripheral nerve blocks (PNBs) over general anesthesia (GA) in a variety of surgical procedures, PNBs can be associated with increased post-operative pain if pain medi...
Detailed Description
As above
Eligibility Criteria
Inclusion
- Undergoing ambulatory surgical procedures that require peripheral nerve blocks for which there is an anticipated post-surgical pain model
- Planned post-discharge analgesic medications including non-steroidal anti-inflammatory drugs, acetaminophen and/or opioids for at least 2 days
- ASA I-III
- Written informed consent
- Have a smartphone device at their disposal
Exclusion
- Inability or refusal to provide informed consent
- Presence of significant cognitive impairment, visual impairments, neurological injury, or psychomotor dysfunction that impairs ability to use the app
- Inability to follow study instructions and complete questionnaires in English
Key Trial Info
Start Date :
December 11 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
March 31 2019
Estimated Enrollment :
29 Patients enrolled
Trial Details
Trial ID
NCT03369392
Start Date
December 11 2017
End Date
March 31 2019
Last Update
April 19 2019
Active Locations (1)
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1
St. Paul's Hospital
Vancouver, British Columbia, Canada, V6Z 1Y6