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

Optical Guided Sentinel Node Biopsy for Staging of Vulvar Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06029504
Acronym
SENTIVUC
Enrollment
115
Registered
2023-09-08
Start date
2023-01-01
Completion date
2027-12-31
Last updated
2023-12-06

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

Conditions

Sentinel Lymph Node, Vulvar Cancer

Brief summary

The aim of this study is to investigate whether Sentinel Node biopsy can be performed without the use of lymphoscintigraphy and with ICG as a mono-tracer in women with vulvar cancer, unifocal tumor \< 4 cm (clinical stage IB and II). Further, to investigate the accuracy of combined PET-CT and ultrasound (US) of the groins with US-guided biopsy of suspicious lymph nodes for the identification of macro-metastases in women with vulvar cancer, unifocal tumor \< 4 cm.

Interventions

None listed

Sponsors

Aarhus University Hospital
CollaboratorOTHER
Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with primary vulva cancer, FIGO stage IB (tumor \< 4 cm) * Patients with unifocal recurrence in the vulva (tumor \< 4 cm) located on the side where the patient is surgically naïve in the groin

Exclusion criteria

* Prior irradiation of the vulva or groins * Prior SNB or inguinal lymphadenectomy in the relevant groin * Known allergy to ICG or iodine (ICG contains 5% sodium iodine)

Design outcomes

Primary

MeasureTime frameDescription
Sentinel Node detection rateThree yearsSN detection rate with ICG and 99mTc-Nanocoll alone perioperatively, where lymphoscintigraphy is blinded, in patients with vulvar cancer (tumor \< 4 cm) without clinical suspicion of metastases to the inguinal lymph nodes.

Secondary

MeasureTime frameDescription
Sensitivity, specificity, PPV and NPVThree yearsSensitivity, specificity, positive predictive value (PPV) and negative predictive value (NPV) of FDG PET-CT and US combined with US-guided biopsy of suspicious lymph nodes for the identification of macro-metastases in the groins

Countries

Denmark

Contacts

Primary ContactLigita P Frøding
ligita.paskeviciute.froeding@regionh.dk+4522722972

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026