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NCT05880797 Clinical Trial

Multidimensional and Multimodal Profiling of Oropharyngeal Carcinoma

Human Papilloma Virus Clinical Trial

Official title:
Multidimensional and Multimodal Profiling of Oropharyngeal Carcinoma

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT05880797
Other study ID # IRB-69452
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 7, 2023
Est. completion date August 2026

Study information
Verified date February 2024
Source Stanford University
Contact Nikita Bedi
Phone (650) 723-5957
Email nbedi@stanford.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to better understand the natural history of oropharyngeal carcinoma (OPC), with or without an association with the human papilloma virus (HPV). For this study, the investigators plan to collect blood from OPC patients prior to treatment and at six subsequent time points.

Recruitment information / eligibility
Status Recruiting
Enrollment 1000
Est. completion date August 2026
Est. primary completion date August 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients diagnosed with oropharyngeal carcinoma or patients with cancer of the unknown primary that is HPV associated, or possibly deemed to be originating from the oropharynx. Exclusion Criteria: - Not willing to sign consent

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
United States Stanford University Palo Alto California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sample collection 30-50cc of blood prior to start of treatment
Primary Sample collection 30-50cc of blood up to 36 months post-op
Secondary tumor sample tumor sample (FFPE) or fresh tissue post-excision or surgery, this will only be collected, if and when feasible, after the tumor has been removed post procedure. Day 1
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