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NCT07044635 · University of Utah

Shortened Course of Radiation Therapy After Trans-oral Robotic Surgery in Patients With HPV-Mediated Oropharyngeal Squamous Cell Carcinoma.

(RAD RAPTORS)

What this study is about

The goal of this study is to evaluate if a shorter course of therapy can improve the quality of life in patients receiving radiation therapy after trans-taken by mouth robotic surgery.

View original scientific description

The goal of this study is to evaluate if a shorter course of therapy can improve the quality of life in patients receiving radiation therapy after trans-oral robotic surgery.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Participant aged ≥ 18 years.
  • Diagnosis of oropharyngeal squamous cell carcinoma.
  • Eligible to receive transoral robotic surgery.
  • If status is known, p16 positivity or HPV positivity by in situ hybridization on pathological sampling of lymph node or primary oropharyngeal tumor. If status not known at the time of step-1 registration, otherwise eligible participants may be enrolled and HPV/p16 status must be determined prior to step-2 registration.
  • Pre-operative TTMV-HPV DNA test collected or is planned to be collected. Pre-operative TTMV-HPV DNA may be collected anytime up until the day of surgery as long as it is prior to surgery.
  • Standard of care tests completed within 60 days of registration may be used for screening.
  • Tests results are not required to confirm eligibility for step 1 registration.
  • ECOG Performance Status ≤ 2
  • Able to provide informed consent and willing to sign an approved consent form that conforms to federal and institutional guidelines.

Exclusion criteria

  • History of prior mucosal head and neck cancer treated with radiation therapy
  • Prior or concurrent malignancy whose natural history or treatment has the potential to interfere with the safety or efficacy assessment of this study
  • Participant has smoked cigarettes within 1 month of registration
  • Prior systemic anti-cancer therapy or any investigational therapy ≤ 14 days or within five half-lives prior to starting study treatment, whichever is shorter.
  • Known distant metastatic disease.
  • Current evidence of any condition that would, in the Investigator's judgment, contraindicate the participant's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, \[participants may not receive the drug through a feeding tube\], social/ psychological issues, etc.)
  • Medical, psychiatric, cognitive, or other conditions that may compromise the participant's ability to understand the participant information, give informed consent, comply with the study protocol or complete the study. Step 2 Registration - Experimental Arm Inclusion Criteria:
  • Completion of trans-oral robotic surgery.
  • Pre- and post-operative TTMV-HPV DNA test results obtained.
  • P16 positivity or HPV positivity by in situ hybridization on pathological sampling of lymph node or primary oropharyngeal tumor
  • For participants of childbearing potential: Negative pregnancy test or evidence of permanent surgical sterilization. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply:
  • \< 50 years of age:
  • Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and
  • Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution
  • ≥ 50 years of age:
  • Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or
  • Had radiation-induced menopause with last menses \>1 year ago; or
  • Had chemotherapy-induced menopause with last menses \>1 year
  • Participants of childbearing potential must agree to use a highly effective method of contraception as described in Section 5.5.2. Exclusion Criteria:
  • Meets ALL of the following criteria for low-risk disease (Note: participants may meet some without being excluded):
  • Pre-operative TTMV-HPV DNA positive
  • Post-operative TTMV-HPV DNA negative
  • Disease: pT1 with ≤ 1 lymph nodes OR pT2N0
  • \<10 pack year smoking
  • No extranodal extension
  • Negative surgical margins
  • No perineural invasion
  • No lymphovascular invasion
  • Meets ANY of the following criteria for high-risk:
  • Post-operative TTMV-HPV DNA positive
  • Surgical margin positive --\>1 mm extranodal extension --≥ 5 lymph nodes
  • Current evidence of any condition that would, in the Investigator's judgment, contraindicate the participant's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, \[participants may not receive the drug through a feeding tube\], social/ psychological issues, etc.) Step 2 Registration - Exploratory Arm Inclusion Criteria
  • Completion of trans-oral robotic surgery.
  • Pre- and post-operative TTMV-HPV DNA test results obtained.
  • Meets ANY of the following criteria:
  • Post-operative TTMV-HPV DNA positive or indeterminate
  • Surgical margin positive
  • \>1 mm extranodal extension
  • ≥5 lymph nodes
  • Pre-operative TTMV-HPV DNA score of ≤ 50
  • For participants of child bearing potential: Negative pregnancy test or evidence of permanent surgical sterilization. The post-menopausal status will be defined as having been amenorrheic for 12 months without an alternative medical cause. The following age-specific requirements apply:
  • \< 50 years of age:
  • Amenorrheic for ≥ 12 months following cessation of exogenous hormonal treatments; and
  • Luteinizing hormone and follicle-stimulating hormone levels in the post-menopausal range for the institution
  • ≥ 50 years of age:
  • Amenorrheic for 12 months or more following cessation of all exogenous hormonal treatments; or
  • Had radiation-induced menopause with last menses \>1 year ago; or
  • Had chemotherapy-induced menopause with last menses \>1 year
  • Participants of childbearing potential must agree to use a highly effective method of contraception as described in Section 5.5.2. Exclusion Criteria
  • Pre-operative TTMV-HPV DNA score of \> 50.
  • Current evidence of any condition that would, in the Investigator's judgment, contraindicate the participant's participation in the clinical study due to safety concerns or compliance with clinical study procedures (e.g., infection/inflammation, intestinal obstruction, unable to swallow medication, \[participants may not receive the drug through a feeding tube\], social/ psychological issues, etc.).

Where

  • Salt Lake City, Utah

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Feb 27, 2026 · Source of record for eligibility and locations

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1 of 42 participants interested
2% interest

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A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

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Study locations

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RECRUITING

Salt Lake City

Utah

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

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Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Oropharyngeal Squamous Cell Carcinoma Treatment in Salt Lake City?

Join others in Utah exploring innovative treatment options through clinical research

Oropharyngeal Squamous Cell Carcinoma Treatment Options in Salt Lake City, Utah

If you're searching for Oropharyngeal Squamous Cell Carcinoma treatment in Salt Lake City, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Salt Lake City and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Oropharyngeal Squamous Cell Carcinoma. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Utah
Now Enrolling
Up to 42 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Oropharyngeal Squamous Cell Carcinoma?

Potential Benefits

  • Access to new treatment approaches before public availability
  • Close monitoring by experienced medical professionals
  • Study-related care provided at no cost
  • Contribute to medical research for Oropharyngeal Squamous Cell Carcinoma

What to Expect

  • Initial screening to determine eligibility
  • Regular check-ups and monitoring visits
  • Possible compensation for time and travel
  • You can withdraw at any time

Frequently Asked Questions About This Oropharyngeal Squamous Cell Carcinoma Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07044635. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.