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sefulness of acellular dermal matrix (Megaderm®) in breast cancer surgery

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0004728
Lead Sponsor
Myongji Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
50
Inclusion Criteria

(1) Female patients aged =19 years
(2) Subjects to treat partial mastectomy or radical surgery of breast and axilla for diagnosis of breast cancer
(3) Patients with breast cancer in stages 0-3
(4) Subjects who needed the using the Megaderm® before primary suture immediately after surgery.
(5) Subject who can follow-up investigation

Exclusion Criteria

(1) 4th stage metastatic or inflammatory breast cancer patient
(2) Patients with infectious diseases, autoimmune disease, and hemostatic disorder
(3) Patients suspected of inflammatory infection in the breast before surgery
(4) Pregnancy
(5) Other, subjects deemed to be in difficulty with clinical research or not required to use Megaderm® by the judgment of the investigator

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Subjective satisfaction score of the cosmetic outcomes
Secondary Outcome Measures
NameTimeMethod
Surgical adverse event and oncology safety with the use of megaderm in surgery
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