CL Item
Did not meet the inclusion/exclusion criteria (F01)
CL Item
Adverse Event (unspecified) (F02)
CL Item
Protocol deviation (unspecified) (F04)
CL Item
Study closed/terminated (unspecified) (F06)
CL Item
Lost to follow up (unspecified) (F07)
CL Item
Investigator discretion, specify (F08)
CL Item
Withdrew consent (unspecified) (F09)