Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Testing the Application of Mepitel Film During Radiation Therapy to Reduce Radiation Related Redness and Peeling in Breast Cancer Patients Following Mastectomy
NCT04989504 · View on ClinicalTrials.gov ↗
Study Summary
This phase III trial studies how well Mepitel Film works in reducing radiation dermatitis (redness and peeling) in patients with breast cancer during radiation therapy after a mastectomy. Mepitel Film may reduce the severity of skin redness and peeling in the area of radiation.
Conditions Studied
Interventions
- OTHER Quality-of-Life Assessment
- OTHER Questionnaire Administration
- OTHER Best Practice
- DEVICE Wound Dressing Material
Study Locations (20)
Iowa
- McFarland Clinic - Ames — Ames
- Mercy Hospital — Cedar Rapids
- Oncology Associates at Mercy Medical Center — Cedar Rapids
- Mercy Cancer Center-West Lakes — Clive
- Iowa Methodist Medical Center — Des Moines
- Medical Oncology and Hematology Associates-Des Moines — Des Moines
- Mercy Medical Center - Des Moines — Des Moines
Delaware
- Beebe South Coastal Health Campus — Frankford
- Helen F Graham Cancer Center — Newark
- Medical Oncology Hematology Consultants PA — Newark
- Beebe Health Campus — Rehoboth Beach
Maine
- MaineHealth Coastal Cancer Treatment Center — Bath
- Maine Medical Center-Bramhall Campus — Portland
- MaineHealth Cancer Care Center of York County — Sanford
- Maine Medical Center- Scarborough Campus — Scarborough
California
- Fremont - Rideout Cancer Center — Marysville
- Gene Upshaw Memorial Tahoe Forest Cancer Center — Truckee
Maryland
- Anne Arundel Medical Center — Annapolis
- University of Maryland/Greenebaum Cancer Center — Baltimore
Florida
- John Fitzgerald Kennedy Medical Center — Atlantis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 216 participants |
| Start Date | 2022-07-26 |
| Est. Completion | 2029-02-15 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04989504
The ClinicalTrials.gov registry entry for NCT04989504 describes a study currently listed as active not recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 216 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alliance for Clinical Trials in Oncology, which has 147 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Breast Carcinoma appearing as the primary indexed condition, and to 4 interventions — of which Quality-of-Life Assessment is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT04989504 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Iowa, Delaware, Maine. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT04989504 about?
NCT04989504 is a clinical study titled "Testing the Application of Mepitel Film During Radiation Therapy to Reduce Radiation Related Redness and Peeling in Breast Cancer Patients Following Mastectomy". This phase III trial studies how well Mepitel Film works in reducing radiation dermatitis (redness and peeling) in patients with breast cancer during radiation therapy after a mastectomy. Mepitel Film may reduce the severity of skin redness and peeling in the area of radiation.
What is the current status of trial NCT04989504?
This trial is currently active not recruiting. It is a Phase 3 study. The enrollment target is 216 participants. The study started on 2022-07-26. Estimated completion is 2029-02-15.
What conditions does trial NCT04989504 study?
This clinical trial studies the following conditions: Breast Carcinoma, Mastectomy Patient. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT04989504?
The interventions under investigation include: Quality-of-Life Assessment (OTHER), Questionnaire Administration (OTHER), Best Practice (OTHER), Wound Dressing Material (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT04989504?
This trial is sponsored by Alliance for Clinical Trials in Oncology, which has 147 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT04989504 being conducted?
This trial has 20 study locations across California, Delaware, Florida, Iowa, Maine. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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