Chronic postsurgical pain (CPSP)
Conditions
Brief summary
Inclusion of a minimum of 15 participants within the study period., Determination of percentage of patients eligible for recruitment who are enrolled and the rate of enrolment., Recording of reasons for declining study participation, if possible., Determination of percentage of completion.
Detailed description
Testing of practical feasibility of the administration method by subcutaneous BTX-A injections in the chest wall evaluated by the percentages of participants completing the intended intervention., Evaluation of tolerability of the intervention during administration and possible side effects/adverse events during follow-up., Determination of questionnaire completion and participation rates at each follow-up assessment time point., Evaluation of “proof of concept” for subcutaneous BTX-A as pain relief in chronic postsurgical pain following surgery for lung cancer, specifically.
Interventions
Sponsors
Aalborg University Hospital
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Inclusion of a minimum of 15 participants within the study period., Determination of percentage of patients eligible for recruitment who are enrolled and the rate of enrolment., Recording of reasons for declining study participation, if possible., Determination of percentage of completion. | — |
Secondary
| Measure | Time frame |
|---|---|
| Testing of practical feasibility of the administration method by subcutaneous BTX-A injections in the chest wall evaluated by the percentages of participants completing the intended intervention., Evaluation of tolerability of the intervention during administration and possible side effects/adverse events during follow-up., Determination of questionnaire completion and participation rates at each follow-up assessment time point., Evaluation of “proof of concept” for subcutaneous BTX-A as pain relief in chronic postsurgical pain following surgery for lung cancer, specifically. | — |
Outcome results
None listed