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Clinical Trials/JPRN-UMIN000032222
JPRN-UMIN000032222
Completed
Phase 2

Phase II trial of sentinel lymph node navigation surgery for patients with early stage endometrial cancer - Phase II trial of sentinel lymph node navigation surgery for patients with early stage endometrial cancer

Department of Obstetrics and Gynecology, Keio University School of Medicine0 sites26 target enrollmentApril 13, 2018

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Not specified
Sponsor
Department of Obstetrics and Gynecology, Keio University School of Medicine
Enrollment
26
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
April 13, 2018
End Date
March 31, 2019
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Department of Obstetrics and Gynecology, Keio University School of Medicine

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) patients who are considered to be regional lymph node metastasis in preoperative diagnostic imaging 2\) patients whith atypical endometrial hyperplasia 3\) patients who are thought to be unbearable by standard surgery including retroperitoneal lymph node dissection due to elderly, past history, complications. 4\) patients with double cancer 5\) patients who have a history of other malignancies. However, excluding cancer patients who do not have cervical carcinoma in situ or who have 5 years or more RFS. 6\) patients who have undergone adnexectomy due to ovarian disease etc. 7\) patients who have undergone surgery for the retroperitoneal region and irradiation of the pelvic and para\-aortic regions due to malignant pelvic tumors 8\) patients who are allergic to indocyanine green (ICG) or RI tracer. 9\) patients who had radiotherapy to the abdomen / pelvic area 10\) patients who had a history of oophorectomy, salpingo\-oophorectomy, salpingectomy due to ovarian or fallopian tube disease 11\) patients who recognize systemic edema and lower limb edema from preoperative period 12\) patients with medical complications with systemic edema 13\) Patients who are difficult to follow up at our hospital.

Outcomes

Primary Outcomes

Not specified

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