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Correlation assessment of Perfusion quantification with Fluobeam and operative outcome in prepectoral implant breast reconstruction: single center, open, prospective observational study

Correlation assessment of Perfusion quantification with Fluobeam and operative outcome in prepectoral implant breast reconstruction: single center, open, prospective observational study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0007054
Enrollment
60
Registered
2022-03-04
Start date
2021-12-02
Completion date
Unknown
Last updated
2022-03-08

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

Conditions

None listed

Interventions

None listed

Sponsors

Seoul National University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients can participate in this study only if they meet all of the following criteria. (1) Patients over 19 years of age (2) Patients who need total mastectomy for breast cancer (3) Patients undergoing immediate two-stage implant breast reconstruction after total mastectomy (skin preservation) is performed. (4) Patients who use Acelluar Dermal Matrix for breast reconstruction (5) Patients who need radiotherapy after breast reconstruction (6) Patients who agree to participate in the study and can be followed up within the study period

Exclusion criteria

Exclusion criteria: Patients with any of the following criteria were excluded from this study. (1) A patient undergoing chemotherapy for cancer other than breast cancer (2) Patients with confirmed local recurrence or systemic metastasis of breast cancer (3) Patients with underlying conditions such as infectious diseases, systemic autoimmune diseases (especially rheumatoid diseases, etc.), and blood coagulation disorders (4) Patients with systemic diseases other than breast cancer (5) Pregnant women or lactating women (6) Other patients who were judged to be difficult to participate in this study by the investigator

Design outcomes

Primary

MeasureTime frame
Skin condition evaluation;Complication evaluation

Secondary

MeasureTime frame
Capsular Contracture;patient satisfaction evaluation

Countries

Korea, Republic of

Contacts

Public ContactKi Yong Hong

Seoul National University Hospital

kyhong@snu.ac.kr+82-2-2072-0310

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026