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Pre-pectoral Breast Reconstruction With or Without Mesh

NCT05888571 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 164

Last updated 2024-01-31

No results posted yet for this study

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.

Conditions

  • Prepectoral Breast Reconstruction
  • TiLOOP Mesh

Interventions

PROCEDURE

prepectoral breast reconstruction

Patients receive immediate prepectoral breast reconstruction

PROCEDURE

Tiloop Mesh implantation

Patients receive immediate prepectoral breast reconstruction with Tiloop Mesh

Sponsors & Collaborators

  • Tianjin Medical University Cancer Institute and Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-07-01
Primary Completion
2026-06-30
Completion
2026-12-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05888571 on ClinicalTrials.gov