First episode Schizophrenia
Item
patients with first-episode of schizophrenia according to dsm-v
boolean
C0439615 (UMLS CUI [1,1])
C0036341 (UMLS CUI [1,2])
Age
Item
aged between18 and 65 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
written informed consent prior to study participation
boolean
C0021430 (UMLS CUI [1])
Comprehension Instructions Research Personnel | Adherence Instructions Research Personnel
Item
subjects who are contractually capable and mentally able to understand and follow the instructions of the study personnel
boolean
C0162340 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
C0035173 (UMLS CUI [1,3])
C1510802 (UMLS CUI [2,1])
C1442085 (UMLS CUI [2,2])
C0035173 (UMLS CUI [2,3])
Study Subject Eligible Magnetic Resonance Imaging
Item
subjects eligible for mri
boolean
C0681850 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0024485 (UMLS CUI [1,3])
Other medical condition Effect Completion of clinical trial | Malignant disease | Epilepsy
Item
the subject has a history of any other illness, which, in the opinion of the investigator, might have an effect on the study performance (e.g. malignant disease, epilepsia)
boolean
C3843040 (UMLS CUI [1,1])
C1280500 (UMLS CUI [1,2])
C2732579 (UMLS CUI [1,3])
C0442867 (UMLS CUI [2])
C0014544 (UMLS CUI [3])
Antipsychotic drug therapy Previous
Item
previous treatment with antipsychotics prior to study participation
boolean
C1319421 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
Metallic material Magnetic Body | Artificial cardiac pacemaker | Piercing
Item
magnetizable metal parts in or at the body, pacemakers, piercings
boolean
C0567346 (UMLS CUI [1,1])
C0563532 (UMLS CUI [1,2])
C0460148 (UMLS CUI [1,3])
C0030163 (UMLS CUI [2])
C0848128 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
pregnant and lactating females
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Institutionalized Person
Item
subject has been committed to an institution by legal or regulatory order
boolean
C0376326 (UMLS CUI [1])
Dependency Investigator | Working Relationship Investigator
Item
dependency or working relationship with the investigator
boolean
C0011546 (UMLS CUI [1,1])
C0035173 (UMLS CUI [1,2])
C0043227 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
C0035173 (UMLS CUI [2,3])
Study Subject Participation Status | Interventional Study
Item
participation in a parallel interventional clinical study
boolean
C2348568 (UMLS CUI [1])
C3274035 (UMLS CUI [2])