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TITLE PAGEProtocol Single dose and Randomized, Single center, Placebo and Active controlled, Crossover Study to Assess the Effect of Omecamtiv Gerbil (OM) on QT/Etc Intervals in Healthy SubjectsProtocol
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01
Review the study protocol to understand the requirements for filling out the randomized open-label single-dose form.
02
Obtain the necessary study materials, including the randomized open-label single-dose form and any accompanying instructions.
03
Enter the participant's information accurately and legibly on the form, including their name, age, gender, and study ID.
04
Randomly assign the participant to the appropriate treatment group according to the study protocol and record this information on the form.
05
Administer the single dose of the assigned treatment to the participant and record the date and time of administration on the form.
06
Monitor the participant for any adverse reactions or side effects following the administration of the treatment and record this information on the form.
07
Complete any additional sections or fields on the form as required by the study protocol.
08
Submit the completed form to the study coordinator or designated personnel for review and processing.
Who needs a randomized open-label single-dose?
01
Participants who are part of a clinical trial or research study that requires the administration of a single dose of a randomized treatment.
02
Investigators and study staff who are responsible for collecting and documenting data related to the administration of the randomized open-label single-dose.
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