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Aimed, Inc. 20 Holyoke Street Cambridge, MA 02138 info@apnimed.comNovember 3, 2022 To: ClinicalTrials.gov This is a cover page to the redacted clinical protocol for APN002 Phase 2, PlaceboControlled,
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Define the research question or hypothesis that you want to evaluate.
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Determine the sample size needed to achieve sufficient statistical power.
03
Randomly assign participants to either the control group or the treatment group.
04
Implement blinding procedures to minimize bias in the study.
05
Monitor and record data on the outcomes of interest for each group.
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Researchers conducting clinical trials to evaluate the efficacy of a new treatment compared to a standard treatment or a placebo.
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Investigators comparing different interventions or strategies to improve patient outcomes in a controlled setting.
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Healthcare professionals seeking evidence-based information to guide clinical decision-making and patient care.
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Parallel-arm study is a type of clinical trial design where two or more treatments are compared in separate arms or groups.
Researchers conducting clinical trials are required to file parallel-arm study to compare.
Parallel-arm study to compare can be filled out by providing detailed information about the study design, treatments being compared, patient inclusion criteria, and outcome measures.
The purpose of parallel-arm study to compare is to evaluate the efficacy and safety of different treatments and determine which is more effective.
Information such as study protocol, informed consent forms, data collection methods, statistical analysis plan, and results must be reported on parallel-arm study to compare.
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