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NCT03416153 · ClinicalTrials.gov registry record · Phase 2

Individualized Adaptive De-escalated Radiotherapy for HPV-related Oropharynx Cancer

A Phase 2 study of Oropharynx Cancer, sponsored by University of Michigan Rogel Cancer Center.

Completed
Registry status
Phase 2
Development phase
91
Enrollment target
2
Study locations

NCT03416153 is a Phase 2 study of Oropharynx Cancer that has completed, run by University of Michigan Rogel Cancer Center. The registered enrollment target is 91 participants, below the 129-participant average among 26 other Oropharynx Cancer trials with a reported enrollment target (29% lower). The trial reports 2 study locations across 1 state.

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The verdict

NCT03416153, a Phase 2 study of Oropharynx Cancer, has completed, sponsored by University of Michigan Rogel Cancer Center.

COMPLETED
Registry status
Phase 2
Development phase
91 participants
Enrollment target
2
Study locations

Study Summary

This prospective study aims to utilize pre- and mid-treatment PET-CT to guide de-escalation of radiation therapy in HPV-related squamous cell carcinoma of the oropharynx.

Conditions Studied

Interventions

  • DRUG Carboplatin
  • DRUG Paclitaxel
  • RADIATION Radiation Therapy

Study Locations (2)

Michigan

  • University of Michigan Hospital - Ann Arbor
  • VA Ann Arbor Healthcare System - Ann Arbor

Trial Details

FieldValue
Enrollment Target 91 participants
Start Date 2018-05-21
Est. Completion 2025-05-05
Phase Phase 2

What the Registry Record Tells You About NCT03416153

The ClinicalTrials.gov registry entry for NCT03416153 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 91 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 129-participant average among 26 other Oropharynx Cancer trials with a reported enrollment target (29% lower). The listed sponsor is University of Michigan Rogel Cancer Center, which has 292 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Oropharynx Cancer appearing as the primary indexed condition, and to 3 interventions - of which Carboplatin is the first listed.

NCT03416153 reports 2 study locations spanning 1 distinct geographic area - top geographies include Michigan.

Frequently Asked Questions

What is clinical trial NCT03416153 about?

NCT03416153 is a clinical study titled "Individualized Adaptive De-escalated Radiotherapy for HPV-related Oropharynx Cancer". This prospective study aims to utilize pre- and mid-treatment PET-CT to guide de-escalation of radiation therapy in HPV-related squamous cell carcinoma of the oropharynx.

What is the current status of trial NCT03416153?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 91 participants. The study started on 2018-05-21. Estimated completion is 2025-05-05.

What conditions does trial NCT03416153 study?

This clinical trial studies the following conditions: Oropharynx Cancer.

What interventions are being tested in trial NCT03416153?

The interventions under investigation include: Carboplatin (DRUG), Paclitaxel (DRUG), Radiation Therapy (RADIATION).

Who is sponsoring clinical trial NCT03416153?

This trial is sponsored by University of Michigan Rogel Cancer Center, which has 292 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03416153 being conducted?

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

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.