A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery
Primary Purpose
Head and Neck Neoplasms
Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
robot assisted endoscopic head and neck surgery using the DaVinci Robotic Surgical System
Sponsored by
About this trial
This is an interventional treatment trial for Head and Neck Neoplasms focused on measuring robotic, robot assisted, minimally invasive, tumors of head and neck
Eligibility Criteria
Inclusion Criteria:
- At least 18 years f age
- Indications for diagnostic or therapeutic approaches for benign or malignant disease of the head and neck
- Written informed consent
Exclusion Criteria:
- Unexplained fever and/or untreated, active infection
- Pregnancy
- Previous head and neck surgery precluding transoral/endoscopic/robotic procedures
- Presence of medical conditions contraindicating general anesthesia or transoral surgical approaches
Sites / Locations
- Montefiore Medical Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
1
Arm Description
robot assisted endoscopic head and neck surgery
Outcomes
Primary Outcome Measures
ability to adequately visualize the operative field and complete planned surgery
Secondary Outcome Measures
complication rate compared to standard endoscopic and minimally invasive procedures
blood loss compared to historical controls of endoscopic and minimally invasive procedures
quality of life at early (1-3 months) and late (one year)
number of days hospitalized immediately after surgery
Time to recurrence of tumor or other pathology for which procedure was performed
Time from start of treatment to death
Full Information
NCT ID
NCT00627562
First Posted
February 5, 2008
Last Updated
March 15, 2016
Sponsor
Montefiore Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT00627562
Brief Title
A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery
Official Title
A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
March 2016
Overall Recruitment Status
Unknown status
Study Start Date
July 2007 (undefined)
Primary Completion Date
June 2014 (Actual)
Study Completion Date
December 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Montefiore Medical Center
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Patients included will have benign or malignant lesions with treatment plan for endoscopic resection or resection by other minimally invasive techniques.
They will be offered a robotic approach to their surgery using the DaVinci robotic surgical system (intuitive Surgical, Inc.).
The objectives are to evaluate our ability to adequately visualize the surgical field and perform the intended surgery without a higher complication rate.
Secondary objective include evaluation of blood loss, length of hospital stay, complications while using the DaVinci robot system, and quality of life in subjects and historical controls undergoing similar surgery without the robot or radiation therapy.
To evaluate recurrence, survival and other outcome data in robotic surgery patients compared with similar historical control groups (matched with respect to stage, prior and subsequent treatment, age, tumor HPV positivity) of patients who have undergone standard surgery without the robot or radiation/chemoradiation treatment as an alternative to surgery.
5. Endpoints will be compared to historical controls.
Detailed Description
The da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) being evaluated in this pilot study consists of 3 basic components: a surgeon's console, articulated mechanical arms and sterilizable instruments. The console includes a computer, video monitor and instrument controls, and is located in the operating room adjacent to the operating room table. The console is connected via computer to the mechanical arms holding the endoscope (surgical TV camera) and sterile surgical tools (e.g., forceps, scissors, electrocautery, etc.). These arms are located immediately adjacent to the patient on the operating room table. The surgeon sits at the console and controls the position and movement of the arms and surgical tools. The design of these tools is based upon well-established, commonly used surgical instruments. The da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) is a "manual image-guided surgery" system that is computer enhanced rather than "computer guided robotic surgery" in which the surgeon programs the computer to do the surgery and the robot does the surgery (also known as a "milling" device).22 Use of the da Vinci® Robotic Surgical System (Intuitive Surgical, Inc., Sunnyvale, CA) in the aforementioned configuration in fact facilitates an exact translation of the surgeon's hand and finger movements at the console to precise and tremor-free movements of the arms and instruments.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Head and Neck Neoplasms
Keywords
robotic, robot assisted, minimally invasive, tumors of head and neck
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
71 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
robot assisted endoscopic head and neck surgery
Intervention Type
Device
Intervention Name(s)
robot assisted endoscopic head and neck surgery using the DaVinci Robotic Surgical System
Intervention Description
Planned endoscopic surgery of the head and neck performed with the DaVinci Robotic Surgical System
Primary Outcome Measure Information:
Title
ability to adequately visualize the operative field and complete planned surgery
Time Frame
1 day
Secondary Outcome Measure Information:
Title
complication rate compared to standard endoscopic and minimally invasive procedures
Time Frame
1 month
Title
blood loss compared to historical controls of endoscopic and minimally invasive procedures
Time Frame
1 day
Title
quality of life at early (1-3 months) and late (one year)
Time Frame
1 year
Title
number of days hospitalized immediately after surgery
Time Frame
at discharge from hospital
Title
Time to recurrence of tumor or other pathology for which procedure was performed
Time Frame
at recurrence of tumor or pathology
Title
Time from start of treatment to death
Time Frame
at time of death
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
At least 18 years f age
Indications for diagnostic or therapeutic approaches for benign or malignant disease of the head and neck
Written informed consent
Exclusion Criteria:
Unexplained fever and/or untreated, active infection
Pregnancy
Previous head and neck surgery precluding transoral/endoscopic/robotic procedures
Presence of medical conditions contraindicating general anesthesia or transoral surgical approaches
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Richard V Smith, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Montefiore Medical Center
City
Bronx
State/Province
New York
ZIP/Postal Code
10467
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
15167030
Citation
Gourin CG, Terris DJ. Surgical robotics in otolaryngology: expanding the technology envelope. Curr Opin Otolaryngol Head Neck Surg. 2004 Jun;12(3):204-8. doi: 10.1097/01.moo.0000122309.13359.af.
Results Reference
background
PubMed Identifier
15933510
Citation
Hockstein NG, Nolan JP, O'Malley BW Jr, Woo YJ. Robot-assisted pharyngeal and laryngeal microsurgery: results of robotic cadaver dissections. Laryngoscope. 2005 Jun;115(6):1003-8. doi: 10.1212/01.WNL.0000164714.90354.7D.
Results Reference
background
PubMed Identifier
16467698
Citation
Hockstein NG, O'Malley BW Jr, Weinstein GS. Assessment of intraoperative safety in transoral robotic surgery. Laryngoscope. 2006 Feb;116(2):165-8. doi: 10.1097/01.mlg.0000199899.00479.75.
Results Reference
background
PubMed Identifier
16366877
Citation
Lobe TE, Wright SK, Irish MS. Novel uses of surgical robotics in head and neck surgery. J Laparoendosc Adv Surg Tech A. 2005 Dec;15(6):647-52. doi: 10.1089/lap.2005.15.647.
Results Reference
background
PubMed Identifier
17011430
Citation
Tanna N, Joshi AS, Glade RS, Zalkind D, Sadeghi N. Da Vinci robot-assisted endocrine surgery: novel applications in otolaryngology. Otolaryngol Head Neck Surg. 2006 Oct;135(4):633-5. doi: 10.1016/j.otohns.2006.07.003. No abstract available.
Results Reference
background
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A Pilot Study of the Use of the DaVinci Robotic System for Otorhinolaryngology-Head and Neck Surgery
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