NODE (groiN ultrasOunD cancEr)

Recruiting now · Not applicable

Conditions studied: Vulvar Cancer Stage Ib, Vulvar Cancer Stage II, Lymph Node Metastasis, Groin Node, Ultrasound Therapy; Complications

In brief

This study is an open label, prospective, experimental, randomised clinical trial. The primary aim of this study is to determine whether it is feasible to randomise vulvar cancer patients into one of two treatment arms:1) surgical groin node dissection (as delivered though either a sentinel node biopsy or inguinofemoral lymph node dissection (IFL), or 2) serial high-resolution bilateral groin ultrasound surveillance and clinical examination every 2 months for 12 months.

Key facts

Study ID

NCT06264167

Run by

Queensland Centre for Gynaecological Cancer

People needed

30

Starts

2024-07-01

Expected to finish

2027-12-31

Last updated by the study team

2026-02-20

Who can join

Age: 18 and older. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women, over 18 years, with histologically confirmed SCC or adenocarcinoma of the vulva
• Clinically stage I or II on medical imaging (CT scan of pelvis, abdomen, and chest), without evidence of regional or distant metastatic disease
• Participant must be suitable to undergo IFL/SNB according to local clinical practice management guidelines
• Signed written informed consent
• Negative serum pregnancy test ≤ 30 days of surgery in pre-menopausal women and women < 2 years after the onset of menopause
• Patient lives within 40 km of a medical diagnostic imaging centre (site investigator approval required for special circumstances)

You may not qualify if…

• Women with non-invasive vulvar conditions (e.g. non-invasive non-mammary Paget's disease)
• Clinical or medical imaging evidence of regional and/or distant metastatic disease
• Serious concomitant systemic disorders incompatible with the study (at the discretion of the investigator)
• Other prior malignancies <5 years before inclusion, except for successfully treated keratinocyte skin cancers, or ductal carcinoma in situ
• Estimated life expectancy of ≤6 months

Where it is running

• St Andrew's War Memorial Hospital — Brisbane, Queensland, Australia (enrolling)
• Royal Brisbane and Women's Hospital — Brisbane, Queensland, Australia (enrolling)
• Buderim Private Hospital — Sunshine Coast, Queensland, Australia (enrolling)
• The Wesley Hospital — Brisbane, Queensland, Australia
• Royal Adelaide Hospital — Adelaide, South Australia, Australia

Full record on ClinicalTrials.gov

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