Active, not recruitingNot applicableNCT05048459
Comparing Two Surveillance Approaches for People Who Have Received Treatment for HPV-associated Head and Neck Cancer and Show No Signs of Disease
Studying Squamous cell carcinoma of the oropharynx
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Memorial Sloan Kettering Cancer Center
- Principal Investigator
- Nancy Lee, MDMemorial Sloan Kettering Cancer Center
- Intervention
- Standard surveillance(other)
- Enrollment
- 40 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2026
Study locations (1)
- Memorial Sloan Kettering Cancer Center (All Protocol Activities), New York, New York, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05048459 on ClinicalTrials.govOther trials for Squamous cell carcinoma of the oropharynx
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