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NRG ONCOLOGY RTCG 0615 A PHASE II STUDY OF CONCURRENT CHEMORADIOTHERAPY USING THREEDIMENSIONAL CONFORMAL RADIOTHERAPY (3DCRT) or INTENSITYMODULATED RADIATION THERAPY (MRT) + (BV) FOR LOCALLY OR REGIONALLY
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To fill out the 0615 master protocol 11-25-14, follow these steps:
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Start by entering the required information in the header section of the form. This includes the study title, study number, and any associated protocol numbers.
03
Next, proceed to the study design section and provide a detailed description of the study design, including any inclusion and exclusion criteria.
04
Move on to the study objectives section and clearly specify the primary and secondary objectives of the study.
05
In the study endpoints section, list all the primary and secondary endpoints that will be evaluated in the study.
06
Provide comprehensive information about the study population in the study population section. This should include details on age, gender, and any other relevant demographics.
07
Fill out the intervention section by describing the study interventions in detail. Include information on dosages, administration methods, and any other relevant details.
08
Complete the study procedures section by listing all the procedures that will be conducted during the study. Mention any specific instruments or tools that will be used.
09
In the adverse events section, describe the procedures for monitoring and reporting adverse events that may occur during the study.
10
Provide detailed information on data analysis and statistical methods that will be employed in the study in the data analysis section.
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Finally, review the completed form for any errors or omissions before submitting it for approval.
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Keep in mind that these are general instructions, and the specific requirements may vary depending on the study and regulatory guidelines.

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The 0615 master protocol 11-25-14 is typically required by researchers, study coordinators, and investigators involved in clinical research studies. It serves as a comprehensive document outlining the study design, objectives, interventions, and procedures for a specific study. Regulatory bodies, ethics committees, and institutional review boards may also require this protocol for approval before the study can begin.
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