Informations:
Erreur:
ID
30520
Description
Combination Deplin® and Antidepressant Therapy for a Major Depressive Episode (MDE)- a Retrospective Analysis; ODM derived from: https://clinicaltrials.gov/show/NCT01001559
Lien
https://clinicaltrials.gov/show/NCT01001559
Mots-clés
Versions (1)
- 11/06/2018 11/06/2018 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
11 juin 2018
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.
Groupe Item commentaires pour :
Item commentaires pour :
Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.
Eligibility Major Depressive Disorder NCT01001559
Eligibility Major Depressive Disorder NCT01001559
- StudyEvent: Eligibility
Similar models
Eligibility Major Depressive Disorder NCT01001559
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age
Item
males or females age 18-70
boolean
C0001779 (UMLS CUI [1])
Arm Active | Major Depressive Disorder CGI - Severity of Illness | Deplin | SSRI | SNRIs | Control Group | Major Depressive Disorder CGI - Severity of Illness | SSRI | SNRIs
Item
the active arm (arm #1) includes randomly selected 100-125 charts of patients with a primary diagnosis of major depression and a cgi-s of ≥4 who began deplin and ssri or snri therapy at the same time beginning in january 2007 to the present; and, control group (arm #2) includes randomly selected 125-150 charts of patients with a primary diagnosis of major depression who began ssri or snri therapy matched in severity (cgi-s of ≥4)
boolean
C1522541 (UMLS CUI [1,1])
C0205177 (UMLS CUI [1,2])
C1269683 (UMLS CUI [2,1])
C3639887 (UMLS CUI [2,2])
C1693359 (UMLS CUI [3])
C0360105 (UMLS CUI [4])
C1579361 (UMLS CUI [5])
C0009932 (UMLS CUI [6])
C1269683 (UMLS CUI [7,1])
C3639887 (UMLS CUI [7,2])
C0360105 (UMLS CUI [8])
C1579361 (UMLS CUI [9])
C0205177 (UMLS CUI [1,2])
C1269683 (UMLS CUI [2,1])
C3639887 (UMLS CUI [2,2])
C1693359 (UMLS CUI [3])
C0360105 (UMLS CUI [4])
C1579361 (UMLS CUI [5])
C0009932 (UMLS CUI [6])
C1269683 (UMLS CUI [7,1])
C3639887 (UMLS CUI [7,2])
C0360105 (UMLS CUI [8])
C1579361 (UMLS CUI [9])
Folic Acid Dosage
Item
folic acid >400 mcg taken at any time during the study
boolean
C0016410 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,2])
Feature Psychotic Depressive episode | Feature Psychotic
Item
psychotic features in the current episode or a history of psychotic features
boolean
C2348519 (UMLS CUI [1,1])
C0033975 (UMLS CUI [1,2])
C0349217 (UMLS CUI [1,3])
C2348519 (UMLS CUI [2,1])
C0033975 (UMLS CUI [2,2])
C0033975 (UMLS CUI [1,2])
C0349217 (UMLS CUI [1,3])
C2348519 (UMLS CUI [2,1])
C0033975 (UMLS CUI [2,2])
Bipolar Disorder | Psychotic Disorders
Item
any bipolar disorder (current or past) or any psychotic disorder (current or past)
boolean
C0005586 (UMLS CUI [1])
C0033975 (UMLS CUI [2])
C0033975 (UMLS CUI [2])
Vagus Nerve Stimulation | Electroconvulsive Therapy | Transcranial magnetic stimulation
Item
current or past treatment with vagus nerve stimulation, ect, or transcranial magnetic stimulation
boolean
C2350432 (UMLS CUI [1])
C0013806 (UMLS CUI [2])
C0436548 (UMLS CUI [3])
C0013806 (UMLS CUI [2])
C0436548 (UMLS CUI [3])
Antipsychotic drug therapy | Antidepressive Agents
Item
antipsychotic therapy in conjunction with their antidepressant currently or in past 4 weeks
boolean
C1319421 (UMLS CUI [1])
C0003289 (UMLS CUI [2])
C0003289 (UMLS CUI [2])