Human Papillomavirus Infection Clinical Trials

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Analysis of HPV DNA in Plasma in Patients With HPV-positive Oropharyngeal Squamous Cell Carcinoma - a Prospective Study of HPV DNA Levels for Treatment Response and Surveillance

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Observational
SUMMARY

The goal of this clinical trial is to determine the value of circulating tumour HPV DNA (human papilloma virus DNA found in the blood) at diagnosis, during treatment, and in the follow-up of patients diagnosed and treated for throat cancer caused by HPV. The main question to answer is if the presence of HPV DNA in the blood one month after the treatment is useful in detecting remaining tumour or relapse within two years after treatment. The participants will be asked to provide blood tests: 1. before treatment 2. weekly during the treatment 3. on all scheduled follow-up appointments 4. on all unplanned appointments where a relapse is suspected

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Only patients with an HPV-positive primary tumour will eventually be eligible for inclusion.

• Non-detectable ctHPVDNA at diagnosis will not be a reason for exclusion.

• Age \>18 years.

• Able to give informed consent.

• The patient will be treated with curative intent.

Locations
Other Locations
Sweden
Dept. of ORL-HNS
RECRUITING
Lund
Contact Information
Primary
Johanna Sjövall, MD, PhD
johanna.sjovall@med.lu.se
+4646172164
Time Frame
Start Date: 2023-05-15
Estimated Completion Date: 2028-05
Participants
Target number of participants: 150
Treatments
Patients with HPV-positive OPC
Patients with HPV-positive OPC. They will provide blood samples before during and after treatment to evaluate treatment response and for early detection of recurrence
Related Therapeutic Areas
Sponsors
Leads: Region Skane

This content was sourced from clinicaltrials.gov