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NRG ONCOLOGY NRGLU001ClinicalTrials.gov NCT02186847RANDOMIZED PHASE II TRIAL OF CONCURRENT CHEMORADIOTHERAPY +/ HCL IN LOCALLY ADVANCED NS CLC This trial is sponsored by the National Cancer Institute
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To fill out the NRG Oncology NRG-LU001 randomized form, follow these steps:
02
Start by filling out your personal information such as name, date of birth, and contact details.
03
Next, provide your medical history including any previous treatments or surgeries related to lung cancer.
04
Answer the questions related to your current health status and any symptoms you may be experiencing.
05
Review and sign the consent form to participate in the NRG-LU001 randomized trial.
06
Submit the completed form to the NRG Oncology team for further processing.

Who needs nrg oncology nrg-lu001 randomized?

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NRG Oncology NRG-LU001 randomized is designed for individuals diagnosed with lung cancer who meet the eligibility criteria set by the trial protocol.
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Patients who are considering or undergoing treatment for lung cancer may be potential candidates for the NRG-LU001 randomized trial.
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It is recommended to consult with your healthcare provider or oncologist to determine if participation in the trial is suitable for your specific case.
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NRG Oncology NRG-LU001 is a clinical trial that focuses on assessing treatment methods for lung cancer, utilizing a randomized approach to evaluate different therapies for their effectiveness.
Investigators and institutions participating in the NRG Oncology NRG-LU001 trial are required to file the necessary documentation and data related to the study.
To fill out the NRG Oncology NRG-LU001 forms, investigators must follow the specific guidelines provided in the trial protocol, ensuring accurate information regarding patient data, treatment details, and outcomes is included.
The purpose of NRG Oncology NRG-LU001 is to evaluate the efficacy and safety of specific treatment modalities for lung cancer patients, improving clinical outcomes and providing data for further research.
Information required to be reported includes patient demographics, treatment regimens, adverse events, efficacy outcomes, and any relevant clinical data as outlined in the trial protocol.
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