interventional
N/A
1 country
1
The objective of this trial is to assess the feasibility of conducting a full-scale clinical trial investigating BTX-A for established CPSP following lung cancer surgery. The trial also aim to explore proof of concept for analgesic effect of BTX-A in surgical lung cancer patients. Primary objectives:
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
Not reported
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
May 21, 2026
Actual (reported)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.
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.
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Region Nordjylland
Gistrup, 9260, Denmark
Clinical trial contact person
First Submitted
May 21, 2026
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Source: European Medicines Agency (EMA), Clinical Trials Information System (CTIS). Original record and public documents are available on CTIS.
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