Surgery for vulvar cancer involves removal of the central tumour as well as groin node dissection as indicated depending on the stage of tumour. Groin node dissection is associated with significant complications including lymphorrea, lymphocyst formation, wound breakdown as well as long term complications including lymphedema. This study has been designed with each patient acting as their own control to investigate if using the PlasmaJet during surgery is associated with a reduction in the above mentioned complications.
Vulvar malignancy is the fourth most common malignancy of the female genital tract. Surgical excision achieves excellent local control and remains the mainstay of treatment. Surgical excision depends on the extent of disease and may be in the form of wide local excision or radical vulvectomy. Lymphadenectomy in the form of bilateral groin node dissection (BGND) is performed for all central tumors with depth of invasion greater than 1 mm, unless there is significant comorbidity contraindicating this, but is known to cause significant postoperative morbidity. Immediate postoperative complications include breakdown and lymphocyst formation in more than 50% of cases. The PlasmaJet is a novel device that produces a jet of pure argon plasma by heating pressurized argon gas. Energy from the argon plasma transfers to tissue as light, heat, and kinetic energy. Following ethical approval, a prospective, crossover, doubleblind, randomized, control trial to assess the PJ system, with the primary outcome being the possibility of reduction in wound breakdown and lymphocyst and lymphedema formation following BGND for vulvar cancer was opened.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
21
The PlasmaJet device is used following groin node dissection on the side randomised to receive it as per protocol specifications
Department of Gynaecological Oncology, Royal Surrey County Hospital NHS Foundation Trust
Guildford, Surrey, United Kingdom
Feasibility of recruitment into the pilot study.The rate (% and absolute rate) of recruitment
Time frame: 24 months
Number of participants with treatment-related adverse events
To document the side-effect profile post-operatively following surgery with the PJ device.
Time frame: Upto 1 year following surgery
Risk of groin lymphorrea/ lymphocyst formation using daily drain outputs
To explore the potential and safety of the PJ device in the prevention of groin lymphocyst formation by prophylactic coagulation of lymph vessels in patients undergoing BGND for vulval cancer
Time frame: Upto 1 year following surgery
Wound Infection
Rate of wound infection following standard surgery vs PlasmaJet use in the groins will be assessed
Time frame: Upto 3months following surgery or till groins healed whichever is sooner
Length of Stay
Length of hospital stay following surgery will be recorded as well as any readmissions
Time frame: Until 14 days following surgery
Lymphedema using the CTC V3.0 grading system
Grade of lymphedema to be assessed at each clinic visit for two years following surgery
Time frame: Upto two years following study entry
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