Oslo University Hospital, Department of Gastrointestinal surgery, The National Hospital
Oslo, 0424, Norway
NCT Number: NCT05129787
230 patients with colorectal cancer liver metastases will be randomly assigned to resection or thermal ablation.
This study is active but is not currently recruiting participants.
Notify Me18 year and older
All sexes
Interventional
Not applicable
Oslo, 0424, Norway
Rationale: The use of thermal ablation of liver tumors is rapidly increasing. This is despite a lack of high-level evidence of the oncologic efficacy of ablation. Ablation is most often used in cases where resection is not possible, but as the technique has improved it is increasingly used as a substitute for resection. A majority of studies on ablation are hampered by selection bias. Selection bias can only be overcome in a randomized controlled trial.
Primary objective:
To compare rates of local tumor progression within 12 months in patients randomly assigned to thermal ablation or surgical resection of colorectal liver metastases.
Secondary objectives:
Study design:
A randomized, controlled, multicenter, double-blinded non-inferiority trial.
Study population:
Two groups of 115 patients (230 in total) with colorectal liver metastasis eligible for radical treatment using EITHER resection OR ablation (not a combination).
Intervention:
Ablation of colorectal liver metastases
Control:
Resection of colorectal liver metastases
Main study parameters/endpoints:
The primary endpoint of the study is local recurrence of cancer at 12 months. Secondary endpoints include overall survival, disease free survival, health related quality of life, postoperative pain, complications, hospital stay and cost-effectiveness.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Resection of metastasis
Ablation of metastasis
Time frame: 12 months
Local tumor progression at site of treatment
Time frame: 60 months
Overall survival following treatment
Time frame: 60 months
A secondary analysis will be performed on a oncologically more homogenous group of patients that fulfil the following requirements: a) no previous surgical procedure on the liver, b) no extrahepatic metastases, and c) that had their primary tumor resected
Time frame: 60 months
DFS
Time frame: 30 days
Morbidity
Time frame: 12 months
HRQoL is measured using SF-36
Time frame: 12 months
An analysis of cost will be performed to assess cost-effectiveness
Time frame: 7 days
The hemodynamic response to the two interventions will be recorded and compared
Time frame: 1 day
The intraoperative movement of the liver will be measured using different ventilation methods (one lung ventilation, jet ventilation, gentle double lung ventilation). The movement of the liver during the different ventilation methods will be assessed in cm.
Time frame: 1 day
Intraoperative cerebral blood flow will be measured and related to cardiac output and other hemodynamic measures. Micro bubbles caused by the treatment will be visualized using ultrasonography.
Time frame: 7 days
The inflammatory response (cytokines, complement, catecholamines) will be compared.
Oslo University Hospital
Other
A Randomized Controlled Trial of Needle Ablation With 3D Verification vs Surgical Resection of Colorectal Cancer Liver Metastases
Acronym: NEW-COMET
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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