CL Item
ADVERSE EVENT (ADVERSE EVENT)
C0877248 (UMLS CUI-1)
C41331 (NCIt V19.10d)
CL Item
COMPLETED (COMPLETED)
C0205197 (UMLS CUI-1)
C25250 (NCIt V19.10d)
CL Item
Recurrent Disease (DISEASE RELAPSE)
C0277556 (UMLS CUI-1)
C38155 (NCIt V19.10d)
CL Item
FAILURE TO MEET CONTINUATION CRITERIA (FAILURE TO MEET CONTINUATION CRITERIA)
C4528356 (UMLS CUI-1)
C139236 (NCIt V19.10d)
CL Item
FAILURE TO MEET RANDOMIZATION CRITERIA (FAILURE TO MEET RANDOMIZATION CRITERIA)
C3642162 (UMLS CUI-1)
C105448 (NCIt V19.10d)
CL Item
LACK OF EFFICACY (LACK OF EFFICACY)
C0235828 (UMLS CUI-1)
C48226 (NCIt V19.10d)
CL Item
LOST TO FOLLOW-UP (LOST TO FOLLOW-UP)
C1302313 (UMLS CUI-1)
C48227 (NCIt V19.10d)
CL Item
Passed Screening But Not Needed; Qualified But Not Needed; Reserve, Not Used (MET ELIGIBILITY CRITERIA BUT NOT NEEDED)
C4726048 (UMLS CUI-1)
C150884 (NCIt V19.10d)
CL Item
NLCB (NO LONGER CLINICALLY BENEFITING)
C4744893 (UMLS CUI-1)
C156551 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH NON-STUDY DEVICE (NON-COMPLIANCE WITH NON-STUDY DEVICE)
C4528360 (UMLS CUI-1)
C139240 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY DEVICE (NON-COMPLIANCE WITH STUDY DEVICE)
C4528361 (UMLS CUI-1)
C139241 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY DRUG (NON-COMPLIANCE WITH STUDY DRUG)
C1709261 (UMLS CUI-1)
C49631 (NCIt V19.10d)
CL Item
NON-COMPLIANCE WITH STUDY SCHEDULE (NON-COMPLIANCE WITH STUDY SCHEDULE)
C5205788 (UMLS CUI-1)
C161411 (NCIt V19.10d)
CL Item
OTHEROther (OTHEROther)
C0205394 (UMLS CUI-1)
C17649 (NCIt V19.10d)
CL Item
PHYSICIAN DECISION (PHYSICIAN DECISION)
C1709536 (UMLS CUI-1)
C48250 (NCIt V19.10d)
CL Item
PREGNANCY (PREGNANCY)
C0032961 (UMLS CUI-1)
C25742 (NCIt V19.10d)
CL Item
Disease Progression; Progressive Disease (PROGRESSIVE DISEASE)
C1335499 (UMLS CUI-1)
C35571 (NCIt V19.10d)
CL Item
PROTOCOL DEVIATION (PROTOCOL DEVIATION)
C1705236 (UMLS CUI-1)
C50996 (NCIt V19.10d)
CL Item
PROTOCOL VIOLATION (PROTOCOL VIOLATION)
C1709750 (UMLS CUI-1)
C142185 (NCIt V19.10d)
CL Item
PROTOCOL-SPECIFIED WITHDRAWAL CRITERION MET (PROTOCOL-SPECIFIED WITHDRAWAL CRITERION MET)
C4684540 (UMLS CUI-1)
C142349 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE (RANDOMIZED BY MISTAKE)
C4528357 (UMLS CUI-1)
C139237 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE WITH STUDY TREATMENT (RANDOMIZED BY MISTAKE WITH STUDY TREATMENT)
C4528358 (UMLS CUI-1)
C139238 (NCIt V19.10d)
CL Item
RANDOMIZED BY MISTAKE WITHOUT STUDY TREATMENT (RANDOMIZED BY MISTAKE WITHOUT STUDY TREATMENT)
C4528359 (UMLS CUI-1)
C139239 (NCIt V19.10d)
CL Item
RECOVERY (RECOVERY)
C2004454 (UMLS CUI-1)
C25746 (NCIt V19.10d)
CL Item
SCREEN FAILURE (SCREEN FAILURE)
C1710476 (UMLS CUI-1)
C49628 (NCIt V19.10d)
CL Item
SITE TERMINATED BY SPONSOR (SITE TERMINATED BY SPONSOR)
C3827772 (UMLS CUI-1)
C106576 (NCIt V19.10d)
CL Item
SPONSOR REQUEST (SPONSOR REQUEST)
C5205787 (UMLS CUI-1)
C161410 (NCIt V19.10d)
CL Item
STUDY TERMINATED BY SPONSOR (STUDY TERMINATED BY SPONSOR)
C1710224 (UMLS CUI-1)
C49632 (NCIt V19.10d)
CL Item
TECHNICAL PROBLEMS (TECHNICAL PROBLEMS)
C1710348 (UMLS CUI-1)
C49633 (NCIt V19.10d)
CL Item
WITHDRAWAL BY PARENT/GUARDIAN (WITHDRAWAL BY PARENT/GUARDIAN)
C3640719 (UMLS CUI-1)
C102355 (NCIt V19.10d)
CL Item
WITHDRAWAL BY SUBJECT (WITHDRAWAL BY SUBJECT)
C1710677 (UMLS CUI-1)
C49634 (NCIt V19.10d)
CL Item
Died (DEATH)
C0011065 (UMLS CUI-1)
C28554 (NCIt V19.10d)
CL Item
ELIGIBILITY CRITERIA MET (ELIGIBILITY CRITERIA MET)
PROTMLST (Comment:en)
C4329786 (UMLS CUI-1)
C132447 (NCIt V19.10d)
CL Item
ENTERED INTO TRIAL (ENTERED INTO TRIAL)
PROTMLST (Comment:en)
C5206987 (UMLS CUI-1)
C161417 (NCIt V19.10d)
CL Item
INFORMED ASSENT OBTAINED (INFORMED ASSENT OBTAINED)
PROTMLST (Comment:en)
C5205794 (UMLS CUI-1)
C161418 (NCIt V19.10d)
CL Item
INFORMED CONSENT OBTAINED (INFORMED CONSENT OBTAINED)
PROTMLST (Comment:en)
C0021430 (UMLS CUI-1)
C16735 (NCIt V19.10d)
CL Item
RANDOMIZED (RANDOMIZED)
PROTMLST (Comment:en)
C3815594 (UMLS CUI-1)
C114209 (NCIt V19.10d)