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Study identifier: NCT05888571 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Pre-pectoral Breast Reconstruction With or Without Mesh

Condition: Prepectoral Breast Reconstruction · TiLOOP Mesh  ·  Sponsor: Tianjin Medical University Cancer Institute and Hospital

PhaseNA
Planned participants164
Who can joinFemale, 18 Years to 65 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Jian Yin  ·  +86-22-23340123  ·  yinjian@tjmuch.com

Chunyong Han  ·  +86-22-23340123  ·  hancy_007@126.com

Always discuss trial participation with your own doctor first.

Locations (1)

Tianjin Medical University Cancer Institute and HospitalTianjin, Tianjin Municipality, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05888571