Using silicone tape to improve scars after abdominal surgery

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial evaluates the effectiveness of silicone tape in improving the appearance of abdominal scars following abdominoplasty in patients undergoing breast reconstruction. Participants will have silicone tape applied to one half of their incision while the other half will receive no dressing, serving as a self-control. The study will follow 32 adult subjects over time to assess scar outcomes and determine if silicone tape provides a significant improvement compared to the standard care. The trial is conducted at the QEII Health Sciences Centre in Halifax, Nova Scotia.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* undergoing de novo abdominoplasty procedures as part of their breast reconstruction

Exclusion Criteria:

* patients with a history of collagen disease, connective tissue disorders, psoriasis or lupus
* patients with scleroderma
* patients with a history of adverse reaction to adhesives or silicone allergy
* patients with signs of dehiscence or infection resulting in modification to the experimental or control dressings
* patients who are unable to care for their incisions
* patients who are current smokers
* patients who are currently on steroids.

Where it's running

• Halifax Infirmary
  Halifax, Nova Scotia, Canada Recruiting

Study contacts

• Principal investigator: Jason G Williams, MD — Nova Scotia Health Authority
• Study coordinator: Jason G Williams, MD
• Email: Jason.Williams@nshealth.ca
• Phone: 902-473-6315

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.