Acute Post-operative Pain Clinical Trial
— PandaOfficial title:
Panda: Evaluation of a Smartphone-based Perioperative Pain Assessment Tool
Verified date | October 2017 |
Source | University of British Columbia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will evaluate Panda, a smartphone-based pain assessment tool. During a child's recovery from surgery, a Post-Anesthetic Care Unit nurse will assess their pain, which helps determine what medication they need. Traditionally, this involves asking the child to rate their pain on a scale from 1 to 10, by moving a slider along a coloured scale or pointing to one of a series of faces on a piece of card. The Panda uses the same methods, but presents them on a smartphone screen. Our evaluation will ensure that the Panda gives the same pain scores as the traditional methods.
Status | Completed |
Enrollment | 144 |
Est. completion date | July 2013 |
Est. primary completion date | July 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 4 Years to 18 Years |
Eligibility |
Inclusion Criteria: - Undergoing a surgical procedure for which there is an anticipated post-surgical pain model - Age 4 - 18 years - ASA I-III, not requiring admission to PICU - Written parental/guardian informed consent and subject informed assent when required (subject age = 7 years) Exclusion Criteria: - Children who have not undergone a surgical procedure (e.g. MRI, X-ray or endoscopy patients) - Inability or refusal to provide informed consent/assent - Developmental delay, neurological injury or psychomotor dysfunction - Children who have a significant visual impairment or have undergone eye surgery |
Country | Name | City | State |
---|---|---|---|
Canada | British Columbia Children's Hospital Department of Anesthesia | Vancouver | British Columbia |
Lead Sponsor | Collaborator |
---|---|
University of British Columbia |
Canada,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Concordance between the electronic and paper versions of the FPS-R and CAS pain scales | The study aims to measure concordance between the (a) pain scores obtained using Panda and pain scores obtained using the Faces Pain Scale-Revised for 4-12 year olds and (b) pain scores obtained using Panda and pain scores obtained using the Coloured Analogue Scale (CAS) for 5-18 year olds. | Up to 2 hours following surgery |
Status | Clinical Trial | Phase | |
---|---|---|---|
Not yet recruiting |
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