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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06415526
Other study ID # 202400581B0
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 3, 2024
Est. completion date May 10, 2024

Study information

Verified date May 2024
Source Chang Gung Memorial Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Current breast cancer surgery is achieving minimally invasive approach to reduce incision while providing better surgical vision and freedom in mastectomy. Breast reconstruction with free deep inferior epigastric artery perforator (DIEP) flap was considered the gold standard, however, the donor site morbidity remains an endless concern. Here we applied robotic-assisted surgery in both mastectomy and free DIEP flap harvest, so-called Oncoplastic Entirely Robot-Assisted Approach (OPERA). A retrospective chart review identified 14 patients with unilateral breast cancer received robotic-assisted mastectomy and robotic assisted free DIEP flap harvest for breast reconstruction. The patient demographics and mastectomy and flap characteristics were reviewed.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date May 10, 2024
Est. primary completion date May 10, 2024
Accepts healthy volunteers
Gender Female
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria: - Patients with ASA (American Society of Anesthesiologist) classification 1-2 - Breast skin should be free from cancer involvement, with adequate tumor to skin distance, and the largest preoperative tumor size no more than 5 cm - The lesion should be located in any of the 4 quadrants away from the nipple, at least 1 cm distance between the lesion and the nipple Exclusion Criteria: - Patients with previous pelvis surgeries (except C-section)

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
OPERA
Robotic-assisted mastectomy and robotic assisted free DIEP flap harvest for breast reconstruction

Locations

Country Name City State
Taiwan Chang Gung Memorial Hospital Taoyuan

Sponsors (1)

Lead Sponsor Collaborator
Chang Gung Memorial Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary ARS incision The length of incision on anterior rectus sheath Intra-operative
Primary Robotic time The time it took to dissect pedicles with robotic arms Intra-operative
Primary Flap size The weight of the flap harvested Intra-operative
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