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Optical Guided Sentinel Node Biopsy for Staging of Vulvar Cancer (SENTIVUC II)

Rigshospitalet logo

Rigshospitalet

Status

Enrolling

Conditions

Sentinel Lymph Node
Vulva Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT06161428
P-2022-946

Details and patient eligibility

About

The aim of the study is to evaluate the feasibility of applying the SLN mapping technique in combination with FDG-PET/CT imaging in women with vulva cancer tumour size >4 cm, multifocal tumors and local recurrences.

Enrollment

100 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with vulva cancer, tumor > 4 cm, multifocal tumor, or local recurrences in vulva

Exclusion criteria

  • Previous external irradiation of the vulva or groins
  • Former sentinel node or inguinal lymphadenectomy in the relevant groin
  • Known allergy to ICG or iodine
  • Patient is in active treatment for other cancer and/or disseminated disease

Trial contacts and locations

1

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Central trial contact

Ligita P Frøding

Data sourced from clinicaltrials.gov

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