Clinical Trials Directory

Trials / Completed

CompletedNCT03369392

PANDA-Regional Feasibility Study of a Smartphone Pain Management Application

The At-home Feasibility Evaluation of PANDA-Regional, a Smartphone Application Designed to Support Post-operative Pain Management in Patients Undergoing Peripheral Nerve Blocks

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
29 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
19 Years – 75 Years
Healthy volunteers
Accepted

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 medications are not taken correctly (titrated). Unfortunately, this is a common occurrence as patients often have difficulty titrating medications in the absence of direct medical care. PANDA, a smartphone-based postoperative pain management tool, is designed to address this issue by helping patients manage their pain medications. The purpose of this study is to demonstrate the feasibility of this application in patients who are discharged after receiving PNBs. The goal is to identify areas of improvement for the application itself. It is hypothesize that PANDA will be successful in supporting patients' postoperative pain management.

Detailed description

As above

Conditions

Interventions

TypeNameDescription
OTHERPanda applicationA smartphone-based postoperative pain management tool

Timeline

Start date
2017-12-11
Primary completion
2019-03-31
Completion
2019-03-31
First posted
2017-12-12
Last updated
2019-04-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT03369392. Inclusion in this directory is not an endorsement.