Transoral Robotic Surgery in Treating Patients With Benign or Malignant Tumors of the Head and Neck
Status: | Recruiting |
---|---|
Conditions: | Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 6/30/2018 |
Start Date: | December 3, 2007 |
End Date: | December 31, 2020 |
Contact: | Ohio State University Comprehensive Cancer Center |
Email: | Jamesline@osumc.edu |
Phone: | 1-800-293-5066 |
A Pilot Study Assessing Transoral Robotic Surgery (TORS) for Oral and Laryngopharyngeal Benign and Malignant Lesions Using the Da Vinci Robotic Surgical System
This pilot clinical trial studies transoral robotic surgery (TORS) in treating patients with
benign or malignant tumors of the head and neck. TORS is a less invasive type of surgery for
head and neck cancer and may have fewer side effects and improve recovery
benign or malignant tumors of the head and neck. TORS is a less invasive type of surgery for
head and neck cancer and may have fewer side effects and improve recovery
To conduct a pilot single-arm study to assess transoral robotic surgery (TORS) for oral and
laryngopharyngeal benign and malignant lesions using the Da Vinci Robotic Surgical System.
laryngopharyngeal benign and malignant lesions using the Da Vinci Robotic Surgical System.
Inclusion Criteria:
- Patient must present with indications for diagnostic or therapeutic approaches for
benign and/or malignant diseases of the oral cavity or laryngopharynx (including the
neoplastic lesions of the tongue, tongue base, retromolar trigone, tonsils, palate,
posterior and lateral pharynx, glottic, supraglottic and subglottic larynx)
- Patients must have adequate transoral exposure of the oral cavity and laryngopharynx
for TORS instrumentation
- Written informed consent and/or Consent waiver by institutional review board (IRB)
Exclusion Criteria:
- Unexplained fever and/or untreated, active infection
- Patient pregnancy
- Previous head and neck surgery that would preclude transoral/robotic procedures. This
is at the investigator's discretion. This is not an exclusion criterion for the
non-surgical arm.
- The presence of medical conditions contraindicating general anesthesia or transoral
surgical approaches
- Inability to grant informed consent
- INTRAOPERATIVE EXCLUSION CRITERIA:
- Inability to adequately visualize anatomy to perform the diagnostic or therapeutic
surgical approach transorally
We found this trial at
1
site
Columbus, Ohio 43210
Principal Investigator: Enver Ozer
Phone: 614-293-8074
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