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PROTOCOL DATE: 2003SEP10 CIC CTG TRIAL: SC.20 AMENDMENT #1: 2004MAY20 AMENDMENT #2: 2005MAR01 AMENDMENT #3: 2005JUL04 AMENDMENT #4: 2006MAR24 ADMINISTRATIVE UPDATE #1: 2006SEP20 AMENDMENT #5: 2009AUG07
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Begin with the patient's information. This includes their full name, date of birth, gender, contact information, and any relevant identification numbers.
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The ncic ctg sc20 protocol is typically used by healthcare professionals involved in clinical trials or research studies. It provides a standardized format for collecting and documenting patient data, ensuring consistency and accuracy in data analysis. Researchers, investigators, physicians, and other healthcare personnel involved in the trial or study may need to familiarize themselves with and use the ncic ctg sc20 protocol.
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NCIC CTG SC20 protocol is a specific protocol used in clinical trials for cancer treatment.
Investigators and institutions involved in the clinical trial are required to file the NCIC CTG SC20 protocol.
The NCIC CTG SC20 protocol can be filled out following the guidelines provided by the National Cancer Institute of Canada Clinical Trials Group.
The purpose of the NCIC CTG SC20 protocol is to outline the details and procedures of a specific clinical trial for cancer treatment.
The NCIC CTG SC20 protocol must include information such as study objectives, eligibility criteria, treatment plan, and data collection methods.
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