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A multicenter prospective cohort study of laparoscopic nipple-areola-sparing mastectomy with immediate pre-pectoral implant and TiLoop Bra mesh versus mesh-free breast reconstruction.

A multicenter prospective cohort study of laparoscopic nipple-areola-sparing mastectomy with immediate pre-pectoral implant and TiLoop Bra mesh versus mesh-free breast reconstruction.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126647
Enrollment
Unknown
Registered
2026-06-12
Start date
2026-06-16
Completion date
Unknown
Last updated
2026-06-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast cancer

Interventions

TiLoop Bra Group:Prepectoral breast reconstruction with implant combined with TiLoop Bra
TiLoop Bra-free group:Prepectoral implant breast reconstruction

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 18-70 years (inclusive); 2. 18 = 0.8-1.0 cm; 7. Willing to undergo breast reconstruction with implants; 8. Able and willing to sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Invasion of breast skin or chest wall; 2.Inflammatory breast cancer; 3.Severe breast ptosis; 4.Macromastia; 5.Patients with diabetes; 6.Patients with a long history of smoking; 7.Patients with serious preoperative diseases, poor general condition, and inability to tolerate surgery; 8.Patients with significantly abnormal immune function;

Design outcomes

Primary

MeasureTime frame
BREAST-Q;—

Countries

China

Contacts

Public ContactLv Qing

West China Hospital of Sichuan University

lvqingwestchina@163.com+86 28 8542 2953

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026