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To Evaluate Plasmajet in Achieving Complete Cytoreduction of Advanced EOC- Initial Feasibility Study

A Pilot Single Blinded Randomized Controlled Trial to Evaluate the Utility and Efficacy of Neutral Argon Plasma as a New Technology in Achieving Complete Cytoreduction of Advanced Epithelial Ovarian Carcinoma- Initial Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02376231
Acronym
PJEOC
Enrollment
120
Registered
2015-03-03
Start date
2013-03-31
Completion date
2017-12-31
Last updated
2019-09-26

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

Conditions

Epithelial Ovarian Cancer

Keywords

EOC Epithelial ovarian cancer, Surgery, nil macroscopic residual disease, Stage 3/4 Epithelial Ovarian Cancer requiring surgery

Brief summary

Surgery for ovarian cancer involves a big cut on your tummy (abdomen) followed by removal of pelvic organs (womb, tubes and ovaries), abdominal organs (fat tissue {omentum}, appendix) and any other tissues involved with cancer. Several studies worldwide have reported that women survive longer and enjoy a longer disease free interval before their disease returns if all visible disease is removed at the time of their surgery. Achieving this is not easy and often there is widespread disease and the surgeons are unable to remove every tumour nodule present as it is attached to the surface of the bowel, diaphragm and other important Extensive surgery with prolonged operating is associated with higher risks. Plasma energy is commonly referred to as the 4th state of matter after solid, liquid and gas. When a gas is heated, it partially or wholly ionizes resulting in high energy particles like ions, electrons and atoms referred to as 'plasma'. PlasmaJet® (PJ) is a new device which uses fine jet of neutral argon plasma from the handpiece that has been shown to have the ability to vaporise nodules close to sensitive organs like the bowel. It may offer the potential to treat the tumour nodules close to sensitive areas like the bowel. There have been no studies exploring its role in vaporising tumour nodules and its impact on survival. The PJ may be used by the surgeon to seal bleeding tissues (coagulate) or to burn away thin layers of tissue (ablate) by vaporization. It is licensed for use to achieve effects of coagulation and ablation. It is similar to conventional surgical devices that are routinely used (called diathermy) to achieve these effects. The PJ however is slightly different in that it may also be used on tissue to vaporise tumour nodules in women with ovarian cancer during surgery though the full extent of this role remains unclear.

Interventions

DEVICESurgery for EOC with trial (PJ) device (PlasmaJet)

Debulking surgery for EOC using PJ device

Sponsors

Dr Thumuluru Kavitha Madhuri
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Imaging+/- Clinical +/- laparoscopic e/o pelvic mass and metastatic disease (FIGO III/IV disease) at presentation. * Confirmation of malignancy on histological/cytological criteria. * All women aged 18 or over with newly diagnosed FIGO stage III to Stage IV EOC undergoing surgical treatment. * All women fit to undergo treatment. * No synchronous malignancy likely to interfere with comparisons. * Written and informed patient consent

Exclusion criteria

* Patient choice * Patient unfit for any treatment modality * Patients who are medically unfit for surgery and would only be suitable for chemotherapy. WITHDRAWAL CRITERIA * Unforeseen complications in the individual patient will be recorded and then analysed. * Life threatening situation to the patient, due to any other unrelated complication. * Patients are free to withdraw from the study at any time with no impact on their care whatsoever.

Design outcomes

Primary

MeasureTime frame
Ability to achieve complete cytoreduction (nil macroscopic residual disease) either with current standard surgery or using PJ.At surgery

Secondary

MeasureTime frameDescription
Post-operative morbidity30 days
Bowel resection rate6months
Stoma formation rate6 months
Per-operative morbidity30 days
Overall Survival5 years
Quality of Life3 yearsQuality of life based on validated EORTC questionnaires
Cost-effectiveness3yearsMeasured as an incremental cost per Quality of Life Year (QALY)
Disease Free Survival3years

Countries

United Kingdom

Outcome results

None listed

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