NCT05888571

Pre-pectoral Breast Reconstruction With or Without Mesh

A Randomized Controlled Trial of Prepectoral Breast Reconstruction With and Without Mesh

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 164 (estimated)
• Sponsor: Tianjin Medical University Cancer Institute and Hospital · Academic / Other
• Sex: Female
• Age: 18 Years – 65 Years
• Healthy volunteers: Not accepted

Summary

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.

Detailed description

The clinical study aims to explore the efficacy and safety that occur after immediate prepectoral breast reconstruction when TiLOOP Mesh is used compared to that not using TiLOOP Mesh.

Conditions

• Prepectoral Breast Reconstruction
• TiLOOP Mesh

Interventions

Type	Name	Description
PROCEDURE	prepectoral breast reconstruction	Patients receive immediate prepectoral breast reconstruction
PROCEDURE	Tiloop Mesh implantation	Patients receive immediate prepectoral breast reconstruction with Tiloop Mesh

Timeline

• Start date: 2023-07-01
• Primary completion: 2026-06-01
• Completion: 2026-12-01
• First posted: 2023-06-05
• Last updated: 2024-01-31

Locations

1 site across 1 country: China