Pre-pectoral Breast Reconstruction With or Without Mesh

Recruiting now · Not applicable

Conditions studied: Prepectoral Breast Reconstruction, TiLOOP Mesh

In brief

To explore the efficacy and safety that occur after immediate prepectoral breast reconstruction when TiLOOP Mesh is used compared to that when TiLOOP Mesh is not used.

Key facts

Study ID

NCT05888571

Run by

Tianjin Medical University Cancer Institute and Hospital

People needed

164

Starts

2023-07-01

Expected to finish

2026-12-01

Last updated by the study team

2024-01-31

Who can join

Age: 18 and older, up to 65. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Adult women aged 18-65 years who plan to undergo unilateral or bilateral immediate prepectoral prothesis breast reconstruction;
• SSM or NSM or Skin-Reducing Mastectomy for breast cancer patients or prophylactic mastectomy;
• Tissue expander size =<800cc, implant size =<600cc;
• The blood perfusion of breast skin flap was well;
• Do not smoking in the last 4 weeks or more
• Patients with normal expectations and mental health for breast reconstruction;
• Signed consent to participate

You may not qualify if…

• Poor perfusion of breast mastectomy flap;
• II stage breast reconstruction patients;
• History of chest radiotherapy;
• BMI greater than 35;
• Patients who have not quit smoking within the last 4 weeks;

Where it is running

• Tianjin Medical University Cancer Institute and Hospital — Tianjin, Tianjin Municipality, China (enrolling)

Full record on ClinicalTrials.gov

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