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NCT05119036 · ClinicalTrials.gov registry record · NA

Adjuvant Treatment Deintensification After Transoral Surgery for Human Papillomavirus-Positive Squamous Cell Carcinoma

A NA study of HPV Positive Oropharyngeal Squamous Cell Carcinoma and Squamous Cell Carcinoma of the Oropharynx, sponsored by Indiana University.

Active
Registry status
NA
Development phase
83
Enrollment target
2
Study locations

NCT05119036: Active NA study of HPV Positive Oropharyngeal Squamous Cell Carcinoma and Squamous Cell Carcinoma of the Oropharynx, sponsored by Indiana University.

NCT05119036 is a NA study of HPV Positive Oropharyngeal Squamous Cell Carcinoma and Squamous Cell Carcinoma of the Oropharynx that is active but no longer recruiting, run by Indiana University. The registered enrollment target is 83 participants, roughly in line with the 87-participant average among 16 other HPV Positive Oropharyngeal Squamous Cell Carcinoma trials with a reported enrollment target. The trial reports 2 study locations across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05119036, a NA study of HPV Positive Oropharyngeal Squamous Cell Carcinoma and Squamous Cell Carcinoma of the Oropharynx, is active but no longer recruiting, sponsored by Indiana University.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
83 participants
Enrollment target
2
Study locations

Study Summary

Oropharyngeal squamous cell carcinoma (OPSCC), commonly known as throat cancer or tonsil cancer, has seen a dramatic rise in incidence over the last twenty years. There are two types of OPSCC: human papillomavirus-positive (HPV+) and human papillomavirus-negative (HPV-). People with OPSCC, regardless of their type, typically receive standard treatment with a combination of chemotherapy, radiation therapy, and surgery. Due to the intensity of standard treatment, survivors may experience unwanted long-term side effects. The goal of this research study is to see if intensifying (stopping or scaling back) treatment still provides the same, or perhaps even better, results when compared to standard treatment.

Primary Outcome

Time from surgery to first disease recurrence or death from any cause

Interventions

  • RADIATION 44 doses of radiation
  • RADIATION 54 doses of radiation

Study Locations (2)

Indiana

  • IU Health Joe and Shelly Schwarz Cancer Center - Carmel
  • Indiana University Melvin and Bren Simon Comprehensive Cancer Center - Indianapolis

Trial Details

FieldValue
Enrollment Target 83 participants
Start Date 2022-05-12
Est. Completion 2026-04
Phase NA
Indiana University

890 total trials

What the registry record for NCT05119036 still lists

NCT05119036 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 83 participants, a relatively small participant target, roughly in line with the 87-participant average among 16 other HPV Positive Oropharyngeal Squamous Cell Carcinoma trials with a reported enrollment target.

The record links to 2 conditions, with HPV Positive Oropharyngeal Squamous Cell Carcinoma appearing as the primary indexed condition, and to 2 interventions - of which 44 doses of radiation is the first listed.

NCT05119036 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT05119036 about?

NCT05119036 is a clinical study titled "Adjuvant Treatment Deintensification After Transoral Surgery for Human Papillomavirus-Positive Squamous Cell Carcinoma". Oropharyngeal squamous cell carcinoma (OPSCC), commonly known as throat cancer or tonsil cancer, has seen a dramatic rise in incidence over the last twenty years. There are two types of OPSCC: human papillomavirus-positive (HPV+) and human papillomavirus-negative (HPV-). People with OPSCC, regardles...

What is the current status of trial NCT05119036?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 83 participants. The study started on 2022-05-12. Estimated completion is 2026-04.

What conditions does trial NCT05119036 study?

This clinical trial studies the following conditions: HPV Positive Oropharyngeal Squamous Cell Carcinoma, Squamous Cell Carcinoma of the Oropharynx.

What interventions are being tested in trial NCT05119036?

The interventions under investigation include: 44 doses of radiation (RADIATION), 54 doses of radiation (RADIATION).

Who is sponsoring clinical trial NCT05119036?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05119036 being conducted?

This trial has 2 study locations across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for HPV Positive Oropharyngeal Squamous Cell Carcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT05119036's enrollment target sits among peer trials

83 8th of 16 higher than 8 of 16 other HPV Positive Oropharyngeal Squamous Cell Carcinoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other HPV Positive Oropharyngeal Squamous Cell Carcinoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT05119036, the US trial registry maintained by the National Library of Medicine. NCT05119036 (small enrollment · single site footprint · active not recruiting) retrieved and formatted by PlainTrial, see methodology.