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Study identifier: NCT06825039 Synced from ClinicalTrials.gov · July 28, 2026
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The Effects of Extracorporeal Shock Wave Therapy in Postsurgical Scars Especially After Abdominplasty and Breast Reduction.

Condition: Scar · Shockwave Therapy  ·  Sponsor: Universiteit Antwerpen

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

Scars can be caused by physical trauma, surgical incisions, burn injuries and even acne. Deep cutaneous injuries induce pathological scars. Other factors, such as mechanical loading, bacterial colonization are potential factors thought to underlie human hypertrophic and keloid scar formation or contractures. The effect may include functional impairment and aesthetic disadvantages. Various non-invasive mechanical interventions of physical scar management (e.g. extracorporeal shock wave therapy or ESWT) could have a beneficial influence on wound healing and prevention of hypertrophic scars. ESWT considerably improves the appearance and symptoms of hypertrophic scars. However, the mechanism underlying the observed beneficial effects is not well understood. The objective of the first part of the study is to elucidate the mechanism underlying changes in cellular mechanosensitive pathways that are induced by ESWT. This review will introduce the histopathological effects on ESWT during wound healing and scar development. The main objective of this study is to determine how much mechanical loading on dermal scars will lead to normal scar healing. The optimal duration, the frequency and the intensity of the applied forces in ESWT to generate a beneficiary effect during different phases of wound healing remains unclear. In this study, biopsies from abdomionplasty postsurgical scars will be examined. Thereby it is possible to evaluate the outcomes on a cellular level through assessin…

This description comes directly from the study's public registry record.

Talk to the study team

Lot Demuynck  ·  +32496204106  ·  lot.demuynck@uantwerpen.be

Ulrike Van Daele

Always discuss trial participation with your own doctor first.

Locations (4)

Ziekenhuis aan de StroomAntwerp, Antwerp, BelgiumRecruiting
Heilig Hart Ziekenhuis LierLier, Antwerp, BelgiumRecruiting
AZ Rivierenland RumstRumst, Antwerp, BelgiumRecruiting
Universitair ZiekenhuisWilrijk, Antwerp, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT06825039