If collected on the CRF, the applicant provides instructions to ensure the data is entered as intended.
Indicate if the subject experienced any medical conditions or events. If Yes, include the appropriate details where indicated on the CRF.
DSCAT
(DSCAT)
DISPOSITION EVENT
2
What is the trial epoch for this disposition event?
Epoch
Select the study epoch for which disposition is being recorded.
EPOCH
(EPOCH)
SCREENING; PRODUCT EXPOSURE; FOLLOW-UP;
3
What was the completion/discontinuation date?
Completion/Discontinuation Date
Record the date that the subject completed the study or study period using this format. If the subject did not complete the study or study period, record the date that the subject discontinued.
Applicant-Defined CRF Completion Instructions
DSSTDTC
4
What was the subject's status?
Status
Document the subject's status for the study or study period. If the subject discontinued prematurely, record the primary reason for discontinuation.
Record all relevant medical conditions or events, as defined in the protocol. Record only one medical condition or event per line. Ensure that the medical conditions or events listed on the Medical History page do not meet any of the exclusion criteria.
DSDECOD
(NCOMPLT)
COMPLETED; ADVERSE EXPERIENCE; DEATH; LOST TO FOLLOW-UP; NON-COMPLIANCE WITH STUDY PRODUCT; PHYSICIAN DECISION; PREGNANCY; PROTOCOL DEVIATION; SITE TERMINATED BY APPLICANT; STUDY TERMINATED BY APPLICANT; WITHDRAWAL BY SUBJECT; OTHER
5
What was the verbatim reason for the subject status?
Specify
If Adverse Experiences, Death, Protocol Deviation or Other is selected from the Status list, provide the verbatim reason.
DSTERM
6
Will the subject continue into the next epoch?
Continue
Record if the subject will be continuing to the next study period of this study.
NOT SUBMITTED
(NY)
No; Yes
7
What is the next epoch the subject will continue to enter?
Next Epoch
Record the planned subsequent study epoch in which the subject intends to participate.