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Participants were considered enrolled in the AHS-2 if they completed an enrollment card signifying their desire to participate in the study.
Subjects who attended this visit were considered enrolled.
Following the informed consent process and assignment of a participant number, volunteers were considered enrolled.
Households with a recorded bucket or chlorine purchase or household visit were considered enrolled in the program (participants).
Patients were considered enrolled in the study and eligible for the final intention to treat analysis at the time of randomization.
Patients were considered "enrolled" in the study once adherence with all inclusion and exclusion criteria had been verified and documented.
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A patient was considered enrolled at the time of randomization.
A participant will be considered enrolled in the study on their day of challenge.
Once the informed consent document has been signed, subjects are considered enrolled in the study.
A volunteer is considered enrolled at the point of receiving the first vaccine (prime).
A patient was considered enrolled if the patient signed the informed consent form and met all eligibility criteria.
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