Shockwave in Postoperative Breast Reconstruction Fibrosis (NCT06919042) | Clinical Trial Compass
RecruitingNot Applicable
Shockwave in Postoperative Breast Reconstruction Fibrosis
United States100 participantsStarted 2024-10-01
Plain-language summary
This study evaluates the potential for extracorporeal shockwave therapy to reduce post-operative soft tissue fibrosis.
Who can participate
Age range18 Years
SexFEMALE
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Inclusion Criteria:
* Subjects greater than 18 years of age.
* Subjects who have undergone plastic surgery procedures and present in the post-operative period with soft tissue firmness suggestive of subcutaneous/parenchymal fibrosis.
Exclusion Criteria:
* Subjects with cardiac pacemakers
* Other medical or psychiatric condition that may increase the risk associated with study participation, may complicate subject compliance, or may interfere with the interpretation of study results and, in the judgment of the Investigator, would make the subject inappropriate for entry into this study.
* Proximity of fibrotic tissue directly adjacent to bone
* Face/neck areas are excluded
* Patients who, in the opinion of the investigator, would not be compliant with the schedule of study visits