Informationen: Dieses ist nicht die aktuellste Version des Datenmodells. Eine Versionsübersicht finden Sie links unter Versionen. Die aktuellste Version finden Sie hier.
Informationen:
Fehler:
ID
20542
Beschreibung
An Eight-Week Study to Evaluate the Efficacy and Safety of SR58611A in Elderly Patients With Depression; ODM derived from: https://clinicaltrials.gov/show/NCT00319709
Link
https://clinicaltrials.gov/show/NCT00319709
Stichworte
Versionen (2)
- 02.03.17 02.03.17 -
- 02.03.17 02.03.17 -
Hochgeladen am
2. März 2017
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY-NC 3.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Depressive Disorder NCT00319709
Eligibility Depressive Disorder NCT00319709
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Depressive Disorder NCT00319709
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Outpatients | inpatient
Item
outpatients or inpatients
boolean
C0029921 (UMLS CUI [1])
C0021562 (UMLS CUI [2])
C0021562 (UMLS CUI [2])
Major Depressive Disorder | Recurrent major depressive episode
Item
major depressive disorder (mdd) with a recurrent major depressive episode (mde) according to dsm iv-tr criteria.
boolean
C1269683 (UMLS CUI [1])
C0154409 (UMLS CUI [2])
C0154409 (UMLS CUI [2])
Montgomery-Asberg Depression Rating Scale Questionnaire
Item
madrs score equal of above 22.
boolean
C4054475 (UMLS CUI [1])
At risk for suicide
Item
patients with a current significant risk of suicide in the investigator's clinical judgment.
boolean
C0563664 (UMLS CUI [1])
Depressive episode Duration
Item
the duration of the current depressive episode is greater than 2 years.
boolean
C0349217 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,2])
Depressive episode Secondary to Medical condition General
Item
patients whose current depressive episode is secondary to a general medical condition
boolean
C0349217 (UMLS CUI [1,1])
C0175668 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
C0205246 (UMLS CUI [1,4])
C0175668 (UMLS CUI [1,2])
C3843040 (UMLS CUI [1,3])
C0205246 (UMLS CUI [1,4])
Bipolar Disorder Lifetime Mini-mental state examination score | Psychotic Disorder Lifetime Mini-mental state examination score | Antisocial Personality Disorder Lifetime Mini-mental state examination score
Item
patients with a lifetime history according to mini at screening of:bipolar disorder, psychotic disorder, antisocial personality disorder.
boolean
C0005586 (UMLS CUI [1,1])
C4071830 (UMLS CUI [1,2])
C2960235 (UMLS CUI [1,3])
C0033975 (UMLS CUI [2,1])
C4071830 (UMLS CUI [2,2])
C2960235 (UMLS CUI [2,3])
C0003431 (UMLS CUI [3,1])
C4071830 (UMLS CUI [3,2])
C2960235 (UMLS CUI [3,3])
C4071830 (UMLS CUI [1,2])
C2960235 (UMLS CUI [1,3])
C0033975 (UMLS CUI [2,1])
C4071830 (UMLS CUI [2,2])
C2960235 (UMLS CUI [2,3])
C0003431 (UMLS CUI [3,1])
C4071830 (UMLS CUI [3,2])
C2960235 (UMLS CUI [3,3])
Anxiety Disorder Mini-mental state examination score | Substance Dependence Mini-mental state examination score | Substance Use Disorders Mini-mental state examination score
Item
patients with a current history according to mini at screening of anxiety disorders, alcohol dependence or abuse or substance dependence or abuse
boolean
C0003469 (UMLS CUI [1,1])
C2960235 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2,1])
C2960235 (UMLS CUI [2,2])
C0038586 (UMLS CUI [3,1])
C2960235 (UMLS CUI [3,2])
C2960235 (UMLS CUI [1,2])
C0038580 (UMLS CUI [2,1])
C2960235 (UMLS CUI [2,2])
C0038586 (UMLS CUI [3,1])
C2960235 (UMLS CUI [3,2])
Comorbidity Severe | Comorbidity Unstable
Item
patients with severe or unstable concomitant medical conditions.
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
C0205082 (UMLS CUI [1,2])
C0009488 (UMLS CUI [2,1])
C0443343 (UMLS CUI [2,2])
Seizures | Childhood seizure febrile single
Item
history of seizures other than a single childhood febrile seizure.
boolean
C0036572 (UMLS CUI [1])
C2733190 (UMLS CUI [2,1])
C0015967 (UMLS CUI [2,2])
C0205171 (UMLS CUI [2,3])
C2733190 (UMLS CUI [2,1])
C0015967 (UMLS CUI [2,2])
C0205171 (UMLS CUI [2,3])
thyroid function abnormal
Item
patients with abnormal thyroid functioning.
boolean
C2242456 (UMLS CUI [1,1])
C0205161 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,2])
ECG finding Clinical Significance
Item
patients with clinically significant ecg findings at screening.
boolean
C0438154 (UMLS CUI [1,1])
C2826293 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,2])
Investigational New Drugs
Item
patients who have taken an investigational drug in the last 3 months prior to screening.
boolean
C0013230 (UMLS CUI [1])
Study Subject Participation Status | amibegron
Item
any subject who has previously participated in a sr58611a protocol.
boolean
C2348568 (UMLS CUI [1])
C2698085 (UMLS CUI [2])
C2698085 (UMLS CUI [2])
Mini-mental state examination score
Item
patients with mini-mental state examination (mmse) score < 25 at screening.
boolean
C2960235 (UMLS CUI [1])