Clin2
NCT05888571Possibly a fitRecruiting

Testing pre-chest breast reconstruction with or without mesh

Prepectoral Breast ReconstructionTiLOOP Mesh

Part of Cancer clinical trials.

This study looks at whether adding mesh (a supportive material) improves results in breast reconstruction placed in front of the chest. It may help some people heal better and get a more comfortable shape, but it depends on your surgery plan and health factors.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
164 people
Ages
18 years to 65 years
Study type
Interventional

Who can take part

  • You are an adult woman between 18 and 65 years old
  • You are planning immediate breast reconstruction on one or both sides, using a pre-chest (front-of-chest) implant or tissue expander
  • Your planned tissue expander is 800 cc or less, and your planned implant is 600 cc or less
  • Your breast skin flap blood flow must be judged as good by the surgical team
  • You have not smoked for at least the last 4 weeks
  • You have a healthy body weight for the study (BMI 35 or lower) and you agree to join

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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