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A prospective study to confirm the effect of preventive lymph node venous anastomosis in gynecological cancer surgery

Not Applicable
Recruiting
Conditions
Neoplasms
Registration Number
KCT0007748
Lead Sponsor
Asan Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
50
Inclusion Criteria

Patients over 20 and under 80 years of age
Patients scheduled for tumor resection and pelvic lymph node dissection for cervical or endometrial or ovarian cancer

Exclusion Criteria

Patients with cervical cancer, endometrial cancer, or ovarian cancer who are scheduled to undergo tumor resection but do not perform Sentinel pelvic lymph node dissection
Patients with indocyanine green (ICG) hypersensitivity
Patients who have not been available for follow-up for more than 18 months

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Incidence of lymphedema
Secondary Outcome Measures
NameTimeMethod
Patient reported outcome measure
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