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NCT04752384 · ClinicalTrials.gov registry record · Phase 2

Transdermal Buprenorphine for the Treatment of Radiation-Induced Mucositis Pain in Head and Neck Cancer Patients

A Phase 2 study, sponsored by Medical College of Wisconsin.

Completed
Registry status
Phase 2
Development phase
20
Enrollment target

NCT04752384: Completed Phase 2 study, sponsored by Medical College of Wisconsin.

NCT04752384 is a Phase 2 study that has completed, run by Medical College of Wisconsin. The registered enrollment target is 20 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04752384, a Phase 2 study, has completed, sponsored by Medical College of Wisconsin.

COMPLETED
Registry status
Phase 2
Development phase
20 participants
Enrollment target

Study Summary

This is a single-arm prospective clinical trial to determine the safety and feasibility of using transdermal buprenorphine in alleviation of radiation induced mucositis pain in head and neck cancer patients.

Primary Outcome

The Brief Pain Inventory - Short Form (BPI-sf) is a nine-item self-administered questionnaire used to evaluate the severity of a patient's pain and the impact of this pain on the patient's daily functioning. The patient is asked to rate their worst, least, average, and current pain intensity -- 0 being no pain and 10 being the pain as bad as you can imagine (within the previous 24 hours).

Interventions

  • DRUG Buprenorphine
  • DRUG Tramadol
  • DEVICE Oral Mucositis (OM) Pain App

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2021-07-08
Est. Completion 2024-04-04
Phase Phase 2
Medical College of Wisconsin

447 total trials

What the finished NCT04752384 record still lists

NCT04752384 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 20 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (85% lower).

The record links to 0 conditions, and to 3 interventions - of which Buprenorphine is the first listed.

NCT04752384 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04752384 about?

NCT04752384 is a clinical study titled "Transdermal Buprenorphine for the Treatment of Radiation-Induced Mucositis Pain in Head and Neck Cancer Patients". This is a single-arm prospective clinical trial to determine the safety and feasibility of using transdermal buprenorphine in alleviation of radiation induced mucositis pain in head and neck cancer patients.

What is the current status of trial NCT04752384?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 20 participants. The study started on 2021-07-08. Estimated completion is 2024-04-04.

What interventions are being tested in trial NCT04752384?

The interventions under investigation include: Buprenorphine (DRUG), Tramadol (DRUG), Oral Mucositis (OM) Pain App (DEVICE).

Who is sponsoring clinical trial NCT04752384?

This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04752384's enrollment target sits among peer trials

20 1805th of 2000 higher than 107 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT04752384, the US trial registry maintained by the National Library of Medicine. NCT04752384 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.