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The verify the accuracy for sentinel lymph node for endometrial cancer(The verify the accuracy for sentinel lymph node for endometrial cancer)

Verify the accuracy for sentinel lymph node in robot-assisted surg ery for endometrial cancer using Indocyanine Greenfluorescence imag ing came ra (The verify the accuracy for sentinel lymph node for endometrial cancer)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs061200004
Enrollment
15
Registered
2020-05-25
Start date
2020-10-16
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Endometrial cancer Endometrial cancer

Interventions

Indocyanine g reen 25mg for injection is dissolved in 5ml of water for injection, and usually 5ml or less is divided into cervical local injections as appropriate. During treatment, indocyanine g ree

Sponsors

Nakamura Keiichiro
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1.Patients who can obtain written consent from their own involuntary research participation 2. Patients with histolog ically confirmed endometrial cancer. 3. Patients who have been confirmed by pelvic MRI examination and/or abdominal /pelvic CT examination as preoperative examination and no patholog ical enlarg ement of lymph nodes 4. Patients scheduled for robot-assisted surg ery for endometrial cancer malig nant tumor 5. Patients ag e 20 to 70 years at the time of reg istration 6. Patients whose g eneral status is 0 or 1 7. Patients with no previous history of radiation therapy, chemotherapy, or surg ery 8.Patients with major org an functions Neutrophil count 2000 / mm3 or more , Hemog lobin 10g / dl or more (correction by blood transfusion is permitted) , Platelet count 100,000 / mm 3 or more , Total bilirubin 1.5mg / dl AST (GOT) and ALT (GPT) 100 IU / l or lessSerum creatinine 1.2mg / dl or less 9. The following tests must be performed within 28 days prior to the operation,The ECG test should not show normal, and abnormal finding s requiring treatment.

Exclusion criteria

Exclusion criteria: 1.Patients with active double cancer (simultaneous double cancer and metachronous double cancer with a disease-free period of 5 years or less). However, lesions equivalent to intraepithelial cancer or intramucosal cancer that are judg ed to be cured by local treatment are not included in active double cancer. 2. Patients with a history of indocyanine g reen sensitivity or iodine sensitivity 3. Patients with severe obesity 4.Patients who are considered difficult to participate in the study due to complications of heart disease and g laucoma 5. Lactating patients

Design outcomes

Primary

MeasureTime frame
False neg ative rate of sentinel lymph node biopsy with indocyanine g reen in endometrial cancer

Secondary

MeasureTime frame
1. Adverse events in indocyanine g reen 2. Incidence of lymphedema

Contacts

Public ContactKeiichiro Nakamura

Okayama University Hospital

k-nakamu@cc.okayama.ac.jp+81-86-235-7320

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026