TriangleNCT00473564 · STUDY IN CONTEXT
Robotic Assisted Surgery in Upper Aerodigestive Tract Surgery
Draft scope assessment: narrower. Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded. Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
Read the full study record and all posted results →
Linked outcomes
Number of participants with adequate exposure and access for use of the da Vinci® Robotic System in oropharyngeal and hypopharyngeal head and neck lesions
Assessment of patient safety evaluating the number of participants who experienced known complications from the use of the da Vinci® Robotic System during surgery, who experienced a need for conversion to open surgery during the procedure, or who required additional surgery for re-excision of the lesion due to positive margins
Reported safety
Quality of life and patient-reported measures
No linked quality-of-life measure is recorded for this setting and study.
Full draft applicability and source-link record
- trial
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- trial label
- Robotic Assisted Surgery in Upper Aerodigestive Tract Surgery
- applicability
- narrower
- applicability note
- Linked by condition-string match at the cancer-entity level. The study's eligibility - stage, biomarker, treatment line and prior therapy - has not been reconciled against this page's definition, so its population is narrower than this page in ways not yet recorded.
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- provenance class
- registry-condition-search
- discovery note
- Found by searching ClinicalTrials.gov for this cancer type, restricted to studies that have posted results to the registry. No FDA notice, FDA label or NCI summary held by this site cites this study. Because the search asked for posted results, studies without posted results were never looked for, so their absence from this page means nothing.
- outcome Count
- 2
- harms Count
- 1
- qol Count
- 0
- outcomes
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- outcome key
- om-0000
- source section id
- NCT00473564-om-0000
- source outcome index
- 0
- endpoint
- Number of Participants With Adequate Exposure and Access to Oropharyngeal and Hypopharyngeal Head and Neck Lesions
- endpoint definition
- Number of participants with adequate exposure and access for use of the da Vinci® Robotic System in oropharyngeal and hypopharyngeal head and neck lesions
- time origin
- Intraoperatively average of 2 hours
- analysis role
- primary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- outcome key
- om-0001
- source section id
- NCT00473564-om-0001
- source outcome index
- 1
- endpoint
- Assessment of Patients Safety by Evaluating the Number of Participants Who Experienced Known Complications From the Use of the da Vinci® Robotic System During Surgery, Experienced a Need for Conversion to Open Surgery or Required Additional Surgery.
- endpoint definition
- Assessment of patient safety evaluating the number of participants who experienced known complications from the use of the da Vinci® Robotic System during surgery, who experienced a need for conversion to open surgery during the procedure, or who required additional surgery for re-excision of the lesion due to positive margins
- time origin
- 3 - 24 months postoperatively
- analysis role
- secondary
- reporting status
- POSTED
- data cutoff
- Source null
- population note
- Participants who successfully underwent transoral robotic-assisted surgery using the da Vinci® Robotic System
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- arms
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- outcome key
- om-0000
- arm key
- OG000
- arm label
- TORS Candidates
- regimen
- Participants who consented to undergo transoral robotic-assisted surgery using the da Vinci® Robotic System
- analyzed count
- 170
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00473564-om-0000#groups/OG000
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- outcome key
- om-0001
- arm key
- OG000
- arm label
- TORS Candidates
- regimen
- Participants who consented to undergo transoral robotic-assisted surgery using the da Vinci® Robotic System
- analyzed count
- 147
- analyzed unit
- Participants
- is comparator
- Source null
- source pointer
- NCT00473564-om-0001#groups/OG000
- harms
- release id
- clinical-indications-draft-1
- disease state id
- ds-hypopharyngeal-cancer
- nct id
- NCT00473564
- harm key
- EG000
- source section id
- NCT00473564-ae
- event group key
- EG000
- event group label
- TORS Candidates
- serious affected
- 21
- serious at risk
- 170
- other affected
- 121
- other at risk
- 170
- frequency threshold
- 5
- collection period
- 30 days
- event definition
- Source null
- undenominated note
- Source null
- curation status
- draft
- reviewed by
- Source null
- reviewed at
- Source null
- created at
- 2026-09-10T00:00:00Z
- quality of life
- setting source links
Preserved source evidence · Not medical advice