Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
24 participants
INTERVENTIONAL
2022-05-01
2025-06-18
Brief Summary
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Detailed Description
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To date, near-infrared fluorescence (NIF)-guided RAMIE using indocyanine green (ICG) dye has not been performed in Canada, and there has been no randomized trial that has compared NIF-guided RAMIE using ICG dye to OTE. In this study, we propose to build the infrastructure for introducing NIF-guided RAMIE using ICG dye to Canada, while laying the foundations for a future randomized controlled trial (RCT) which will compare it to OTE. This study is a Phase I, single center, prospective feasibility randomized controlled trial with two phases: Phase A: Learning Curve of NIF-guided RAMIE using ICG dye; and Phase B: A Randomized Controlled Feasibility Trial. In Phase A, 40 patients will be enrolled, and they will all undergo NIF-guided RAMIE using ICG dye. Evidence shows that a surgeon experienced in MIE requires experience of 40 cases to gain proficiency of RAMIE. In Phase B, 54 patients will be enrolled, and they will be randomized to either NIF-guided RAMIE using ICG dye, or OTE.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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NIF-Guided RAMIE using ICG Dye (Experimental Arm)
The patient will undergo NIF-guided RAMIE using ICG dye using the standard Ivor-Lewis approach. This will be a two-stage operation involving a first stage through a 5-port robotic approach through the abdomen to achieve a proximal gastrectomy and D2 nodal dissection. A feeding jejunostomy would not be inserted, as per the enhanced recovery pathway for esophagectomy. In addition, the vascularization of the conduit can be confirmed using the near-infrared camera of the robot with the ICG dye. The second stage of the operation will involve a 4-port robotic approach through the right chest to achieve thoracic nodal dissection, esophagectomy, and a hand-sewn anastomosis between the residual esophagus and the gastric conduit at the level of the azygous vein. During this second stage of the operation, NIF with ICG dye will be used to visualize the vascular supply of the gastric conduit, and assess the gastric conduit for any perfusions to potentially reduce anastomotic leaks.
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE)
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE) will be performed using the Da Vinci Robotic Surgical Platform.
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE)
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE) will be performed using the Da Vinci Robotic Surgical Platform.
Open Transthoracic Esophagectomy (OTE)
The patient will undergo OTE using the standard Ivor-Lewis approach. This is a two-stage operation involving a first stage through laparotomy, proximal gastrectomy, D2 nodal dissection, and insertion of feeding jejunostomy. The second stage of the operation will involve a right thoracotomy, thoracic nodal dissection, esophagectomy, and a stapled anastomosis between the residual esophagus and the gastric conduit at the level of the azygous vein.
Open Transthoracic Esophagectomy (OTE)
Open Transthoracic Esophagectomy (OTE) is the current standard of care.
Interventions
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Robotic Assisted Minimally Invasive Esophagectomy (RAMIE)
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE) will be performed using the Da Vinci Robotic Surgical Platform.
Open Transthoracic Esophagectomy (OTE)
Open Transthoracic Esophagectomy (OTE) is the current standard of care.
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE)
Robotic Assisted Minimally Invasive Esophagectomy (RAMIE) will be performed using the Da Vinci Robotic Surgical Platform.
Eligibility Criteria
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Inclusion Criteria
* Clinical Stage I, II, or III esophageal cancer, who are candidates for surgery after discussion in multidisciplinary tumor board.
* Candidates for minimally invasive surgery as determined by the operating surgeon.
Exclusion Criteria
* Women who are currently pregnant or are breastfeeding; or women of childbearing potential who are not currently taking adequate birth control
* Clinical Stage IV esophageal cancer.
* Not a candidate for minimally invasive surgery as determined by the operating surgeon.
18 Years
ALL
No
Sponsors
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McMaster University
OTHER
St. Joseph's Healthcare Hamilton
OTHER
Responsible Party
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Wael Hanna
Associate Professor
Locations
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St. Joseph's Healthcare Hamilton
Hamilton, Ontario, Canada
Countries
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Other Identifiers
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SJHH_RAMIE_vs_OTE_Feasibility
Identifier Type: -
Identifier Source: org_study_id
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