Assessing the da Vinci® Robotic Surgical System for Surgery of the Upper Aerodigestive Tract
Primary Purpose
Hypopharyngeal Neoplasms, Laryngeal Neoplasms, Head and Neck Cancers
Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
da Vinci Surgical Robot Platform
Transoral Robotic Surgery
Sponsored by
About this trial
This is an interventional health services research trial for Hypopharyngeal Neoplasms
Eligibility Criteria
Inclusion Criteria:
- Patient or volunteer is 18 years of age or older
- Patients must have indication for diagnosis and/or therapy of diseases of the oropharynx, hypopharynx, and/or larynx.
Exclusion Criteria:
- unexplained fever and/or untreated
- active infection
- pregnancy
anatomic parameters which preclude transoral surgery, such as:
- trismus
- limited range of neck motion
- poor dentition
- redundant hypopharyngeal or supraglottic tissue which would prevent adequate visualization of the tumor
- participation in a research protocol which precludes participation in other protocols
Sites / Locations
- Stanford University School of Medicine
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Transoral Robotic Surgery
Arm Description
Pilot study; single arm - use of da Vinci Surgical Robot Platform to access neoplastic disease of the upper aerodigestive tract.
Outcomes
Primary Outcome Measures
Overall Complication Rate (Intraoperative and Postoperative)
Complications encountered intraoperatively or up to six weeks postoperatively. This would include injury to patient, hemorrhage, lacerations, and readmission following surgery.
Secondary Outcome Measures
Feasibility Defined as Ability to Perform the Planned Diagnostic or Therapeutic Procedure
Average Blood Loss
Blood lost during procedure
Average Operative Time
Average operative time in minutes
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00721539
Brief Title
Assessing the da Vinci® Robotic Surgical System for Surgery of the Upper Aerodigestive Tract
Official Title
A Pilot Study Assessing Transoral Robotic Surgery (TORS) For Oral And Laryngopharyngeal Benign And Malignant Lesions Using The da Vinci® Robotic Surgical System
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Terminated
Why Stopped
Low Accrual
Study Start Date
September 2010 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
September 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To assess the use of the da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) in transoral surgeries in patients with benign and malignant lesions of the oral cavity and laryngopharynx.
Detailed Description
In the past two decades the interest in minimally invasive techniques for transoral treatment of head and neck benign and malignant lesions has been growing due to the decreased morbidity of transoral approaches, and some surgeons have been moving away from traditional open resections. Transoral resection of neoplasms of the upper aerodigestive, by its minimally invasive nature, may afford a shorter hospitalization and recovery time for patients when compared to those patients who undergo traditional "open" surgery. In surgery of the oropharynx, hypopharynx, and larynx, transoral endoscopic surgery can provide similar outcomes in terms of local control of disease when compared to open procedures, while improving time to restoration of oral intake and shortening time to tracheostomy decannulation. Therefore, in select patients, a transoral surgical approach may afford clear advantages over traditional open approaches. Current techniques, however, are limited by the inability to attain direct line of site exposure of the lesion. Use of robot-assisted technology as a means to overcome surgical limitations, to provide surgeons with improved dexterity and precision, and to couple advanced imaging techniques with three-dimensional depth perception, may allow for the completion of transoral surgical approaches in patients for whom conventional technology has been suboptimal.
The da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) is FDA-approved for use in a variety of laparoscopic, thoracoscopic, cardiac, and urologic surgical procedures. This protocol will assess the use of the da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) in transoral surgeries in patients with benign and malignant lesions of the oral cavity and laryngopharynx. Traditional endoscopic removal of tumors of the oropharynx and laryngopharynx is usually preferred to traditional open resection because of the decrease in morbidity and improved functional outcomes experienced by patients. The limiting step in these procedures has been exposure of, visualization of, and access to candidate tumors. The da Vinci surgical system offers the possibility of significant improvements in exposure, visualization and access to these candidate tumors with no added risk to patients. Overall this may significantly increase the number of patients who are candidates for endoscopic surgery. Alternative procedures will include traditional open surgical removal of tumors as well as traditional endoscopic removal of tumors using the microscope and CO2 laser. Open surgical approaches are reserved for patients who have large tumors unsuitable for endoscopic removal or in whom endoscopic visualization of the tumor is inadequate or impossible. The da Vinci surgical system would offer improved visualization of tumors that might otherwise be inaccessible to a traditional endoscopic approach.
Candidate patients will present with a neoplasm of the oropharynx, hypopharynx or larynx. Those patients assessed preoperatively to be candidates for transoral surgery (eg, Mallampati class I or II, normal range of neck motion, no trismus) will undergo surgery via a transoral approach to resect the tumor. This will require general anesthesia and may require postoperative hospitalization. If the tumor can be accessed, resection will proceed using the da Vinci robot. In whom the tumor cannot be accessed, resection will proceed via the conventional open approach. Pre and postoperative care will not be affected by this protocol, as it deals strictly with the manner in which the tumor is removed. Postoperative care and visits are standardized as to the nature of the tumor (eg, malignant tumors usually require follow-up visits every four to six weeks to monitor for tumor recurrence). Complications, blood loss, operative time, length of hospitalization, time to resumption of oral intake, time to decannulation, and overall local control rates will be assessed in the postoperative period.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypopharyngeal Neoplasms, Laryngeal Neoplasms, Head and Neck Cancers
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Transoral Robotic Surgery
Arm Type
Other
Arm Description
Pilot study; single arm - use of da Vinci Surgical Robot Platform to access neoplastic disease of the upper aerodigestive tract.
Intervention Type
Device
Intervention Name(s)
da Vinci Surgical Robot Platform
Intervention Description
daVinci Surgical Robot Platform is a surgical device that enhances transoral access to the upper aerodigestive tract through miniaturization of endoscopes and micromanipulators that can be introduced through the mouth.
Intervention Type
Procedure
Intervention Name(s)
Transoral Robotic Surgery
Intervention Description
Eligible patients will undergo transoral treatment of neoplastic disease of the upper aerodigestive tract using the daVinci Surgical Robot Platform as opposed to traditional (TOL - transoral laser; TEC - transoral electrocautery) methods.
Primary Outcome Measure Information:
Title
Overall Complication Rate (Intraoperative and Postoperative)
Description
Complications encountered intraoperatively or up to six weeks postoperatively. This would include injury to patient, hemorrhage, lacerations, and readmission following surgery.
Time Frame
Six weeks
Secondary Outcome Measure Information:
Title
Feasibility Defined as Ability to Perform the Planned Diagnostic or Therapeutic Procedure
Time Frame
Six weeks
Title
Average Blood Loss
Description
Blood lost during procedure
Time Frame
Duration of procedure up to two hours
Title
Average Operative Time
Description
Average operative time in minutes
Time Frame
Up to four hours (240 minutes)
10. Eligibility
Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient or volunteer is 18 years of age or older
Patients must have indication for diagnosis and/or therapy of diseases of the oropharynx, hypopharynx, and/or larynx.
Exclusion Criteria:
unexplained fever and/or untreated
active infection
pregnancy
anatomic parameters which preclude transoral surgery, such as:
trismus
limited range of neck motion
poor dentition
redundant hypopharyngeal or supraglottic tissue which would prevent adequate visualization of the tumor
participation in a research protocol which precludes participation in other protocols
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edward J. Damrose MD, FACS
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Stanford University School of Medicine
City
Stanford
State/Province
California
ZIP/Postal Code
94305
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Assessing the da Vinci® Robotic Surgical System for Surgery of the Upper Aerodigestive Tract
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