Clinical trial

The Feasibility of Assessing Economic Costs of the Signia Stapler Versus Vessel Sealer Extend Energy Device With SureForm Stapling in Robotic-Assisted Segmentectomy for Lung Cancer

Name
15910
Description
Robotic-assisted thoracoscopic surgery (RTS) segmentectomy is safe and effective for patients with early-stage non-small cell lung cancer (NSCLC). In RTS-segmentectomy, dissection and sealing procedures are performed by either staplers or energy devices. Staplers, the current standard of care, have been associated with higher operating costs compared to energy devices for open lobectomy, RTS lobectomy and minimally invasive segmentectomy. However, there is a lack of prospective research evaluating the costs of the two methods for lung dissection and vessel sealing in RTS-segmentectomy. This prospective trial seeks to determine whether it is feasible to conduct a randomized controlled trial evaluating the costs of the Signia stapler versus Vessel Sealer Extend energy device in RTS-segmentectomy for NSCLC. If this trial is feasible, we will be able to conduct a full-scale trial to compare costs and health outcomes, providing an economic evaluation that will inform hospital decision makers and clinicians in Canada.
Trial arms
Trial start
2023-04-14
Estimated PCD
2024-04-30
Trial end
2024-04-30
Status
Recruiting
Treatment
Medtronic Signia Stapler
The Signia Stapler is a powered stapler that can be used for tissue dissection and vessel sealing during surgery.
Arms:
Medtronic Signia Stapler
Da Vinci Vessel Sealer Extend Energy Device with SureForm Stapling
The Vessel Sealer Extend Energy Device is integrated with the da Vinci system and uses bipolar energy technology to facilitate tissue dissection and vessel sealing.
Arms:
Da Vinci Vessel Sealer Extend Energy Device with SureForm Stapling
Size
50
Primary endpoint
Feasibility and safety
Up to 3 weeks post-surgery
Recruitment
Up to 8 weeks after recruitment first opens
Randomization
Baseline
Data collection of stapler reload model
Up to 3 weeks post-surgery
Data collection of stapler quantities
Up to 3 weeks post-surgery
Data collection of energy sealing data
Up to 3 weeks post-surgery
Data collection of energy device data
Up to 3 weeks post-surgery
Eligibility criteria
Inclusion Criteria: * Age between 18 and 120 years at time of consent * Ability to speak and understand English * Clinical stage I, II or IIIa NSCLC * Candidate for RTS segmentectomy, as determined by the operating surgeon Exclusion Criteria: * Anticoagulation with inability to cease anticoagulant therapy prior to surgery * Incurable coagulopathy * Systemic vascular disease or vasculitis * Not a candidate for RTS segmentectomy
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}}, 'enrollmentInfo': {'count': 50, 'type': 'ESTIMATED'}}
Updated at
2024-03-29

1 organization

1 product

3 indications

Indication
lung cancer
Indication
Thoracic Cancer
Indication
Lung Neoplasm