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Completed

NCT Number: NCT03049280

Prospective, Multicenter da Vinci® SP™ Surgical System TORS Study

A prospective, multicenter investigation of the da Vinci® SP™ Surgical System in Transoral Robotic Surgery (TORS) procedures for malignant oropharyngeal tumors.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Board of Trustees of the Leland Stanford Junior University, Palo Alto, California, United States

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About this study

A prospective, multicenter investigation to evaluate the safety and clinical performance of the da Vinci SP Surgical System, instruments, and accessories in TORS procedures for malignant oropharyngeal tumors classified as T1 and T2.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • T1 or T2 malignant oropharyngeal tumor
  • Tumor amenable to transoral resection
  • No previous treatment for the index tumor
  • Willing and able to provide written informed consent
  • Willing and able to comply with the study protocol requirements

Exclusion criteria

  • T3 or T4 stage tumor
  • Previous radiation treatment to the head and neck, with or without chemotherapy
  • Evidence of other primary cancers or distant metastasis or subject with synchronous primary tumor excluding skin cancers
  • Pre-operative expectation of needing microvascular soft-tissue reconstruction
  • Tumor that invades and/or abuts the internal and/or external carotid artery
  • Retropharyngeal carotid artery coincident with a tonsillar cancer or posterior pharyngeal wall cancer
  • Evidence of mandibular invasion of tumor
  • Eastern Cooperative Oncology Group Performance Status score greater than or equal to 2
  • On a medication that interferes with clotting that cannot be stopped prior to surgery
  • Contraindication for general anesthesia or surgery
  • Mentally handicapped or has psychological disorder or severe systemic illness that would preclude compliance with study requirements or ability to provide informed consent
  • Pregnant or suspected to be pregnant

Treatment and study plan

Transoral robotic surgery

Device

Transoral robotic surgery for T1 & T2 oropharyngeal cancers

Primary outcomes

  1. Performance

    Time frame: Intraoperative

    Performance defined as the conversion to an open approach required to complete the procedure

  2. Number of Subjects With Device-related Serious Adverse Events

    Time frame: Intraoperative period

    Safety is determined by measuring the number of subjects that experience device-related serious adverse events

Secondary outcomes

  1. Positive Surgical Margin

    Time frame: Through14-days postoperatively

    Rate of final positive surgical margins confirmed by pathology

Sponsors and collaborators

Lead sponsor

Intuitive Surgical

Industry

Registry information

Official study title

A Prospective, Multicenter Investigation of the da Vinci® SP™ Surgical System in TORS Procedures for Resection of Malignant Tumors

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Feb 10, 2017
Registry last updated
Oct 6, 2020

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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