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Terminated Phase 3 Interventional Results available

Testing the Addition of Targeted Radiation Therapy to Surgery and the Usual Chemotherapy Treatment (Pemetrexed and Cisplatin [or Carboplatin]) for Stage I-IIIA Malignant Pleural Mesothelioma

ClinicalTrials.gov ID: NCT04158141

Public ClinicalTrials.gov record NCT04158141. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 10:37 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase III Randomized Trial of Pleurectomy/Decortication Plus Systemic Therapy With or Without Adjuvant Hemithoracic Intensity-Modulated Pleural Radiation Therapy (IMPRINT) for Malignant Pleural Mesothelioma (MPM)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial studies how well the addition of targeted radiation therapy to surgery and the usual chemotherapy treatment works for the treatment of stage I-IIIA malignant pleural mesothelioma. Targeted radiation therapy such as intensity-modulated radiation therapy or pencil beam scanning uses high energy rays to kill tumor cells and shrink tumors. Drugs used in chemotherapy, such as pemetrexed, cisplatin, and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving targeted radiation therapy in addition to surgery and chemotherapy may work better than surgery and chemotherapy alone for the treatment of malignant pleural mesothelioma.

Study identification

NCT ID
NCT04158141
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
NRG Oncology
Other
Enrollment
16 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 28, 2020
Primary completion
Nov 19, 2023
Completion
Nov 19, 2023
Last update posted
Jul 12, 2026

2020 – 2023

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
10
Facility City State ZIP Site status
UM Sylvester Comprehensive Cancer Center at Coral Gables Coral Gables Florida 33146
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Mayo Clinic in Rochester Rochester Minnesota 55905
Memorial Sloan Kettering Cancer Center New York New York 10065
Ohio State University Comprehensive Cancer Center Columbus Ohio 43210
MD Anderson in The Woodlands Conroe Texas 77384
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston Texas 77030
UT MD Anderson Cancer Center Houston Texas 77030
MD Anderson West Houston Houston Texas 77079
UT MD Anderson - League City League City Texas 77573
MD Anderson in Sugar Land Sugar Land Texas 77478
Swedish Medical Center-First Hill Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04158141, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 12, 2026 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT04158141 live on ClinicalTrials.gov.

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