ID

29792

Descrizione

Study ID: 101464 Clinical Study ID: SCA101464 Study Title: A Multicenter, Randomized, Double-Blind, Parallel Group Study to Evaluate the Efficacy and Safety of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive Therapy to an Atypical Antipsychotic Agent(s) in Subjects with Schizophrenia Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00086593 https://clinicaltrials.gov/ct2/show/NCT00086593 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lamotrigine Study Indication: Lamictal XR,Lamictal,LAMICTIN This ODM form contains Concomitant Medications.

collegamento

https://clinicaltrials.gov/ct2/show/NCT00086593

Keywords

versioni (1)
  1. 19/04/18 19/04/18 - Sarah Riepenhausen
Titolare del copyright

GlaxoSmithKline

Caricato su

19 aprile 2018

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0
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Evaluation of a Flexible Dose of Lamotrigine Compared to Placebo as an Adjunctive to Atypical Antipsychotic Agents in Schizophrenia NCT00086593

Inglese

Concomitant Medications

1 moduli  
Concomitant Medications
Descrizione

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Were any concomitant medications taken by the subject during the study?
Descrizione

If Yes, complete the other Items of this Itemgroup.

Tipo di dati

text

Alias
UMLS CUI [1]
C2347852
Drug Name
Descrizione

Record over-the-counter and prescription drugs prescribed. Trade names are preferred for all medications; this is particularly encouraged for all combination medications, e.g., multivitamins and cold medications. The subject should be encouraged to disclose all medications he/she is taking, including non-prescribed medications, herbal remedies, and nutritional supplements. If the subject is female, cross-check with the DEMOGRAPHY FOR FEMALES page that any contraceptive drugs taken by the subject are recorded.

Tipo di dati

text

Alias
UMLS CUI [1]
C2360065
Dose
Descrizione

Dose

Tipo di dati

float

Alias
UMLS CUI [1]
C3174092
Units
Descrizione

Units

Tipo di dati

text

Alias
UMLS CUI [1]
C2826646
Frequency
Descrizione

Frequency

Tipo di dati

text

Alias
UMLS CUI [1]
C2826654
Route
Descrizione

Route

Tipo di dati

text

Alias
UMLS CUI [1]
C2826730
Date Started
Descrizione

If the concomitant medication start date is prior to the study start date, affirm ‘Was medication started pre-study?’.

Tipo di dati

date

Alias
UMLS CUI [1]
C2826734
Was medication started pre-study?
Descrizione

If a concomitant medication was started pre-study, check that the indication is recorded on the CURRENT MEDICAL CONDITIONS page.

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2981448
Date stopped
Descrizione

Record the stop date if concomitant medication is stopped prior to the end of the study. If the subject is to continue taking the concomitant medication after the study is over, affirm ‘Was medication continued post-study?’.

Tipo di dati

date

Alias
UMLS CUI [1]
C2826744
Was medication continued post-study?
Descrizione

Ongoing Medication

Tipo di dati

boolean

Alias
UMLS CUI [1]
C2826666
Conditions treated / Indication
Descrizione

Conditions treated / Indication

Tipo di dati

text

Alias
UMLS CUI [1]
C2826696
Prophylaxis?
Descrizione

Prophylaxis

Tipo di dati

text

Alias
UMLS CUI [1]
C0199176
Was drug administered for an adverse event?
Descrizione

If the concomitant medication was taken for an adverse event, check that the event is entered on the appropriate ADVERSE EVENTS page(s) and that the dates are consistent with the event.

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0877248
UMLS CUI [1,2]
C2347852
Was drug administered as a rescue medication?
Descrizione

Rescue medication

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0884980
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Similar models

Concomitant Medications

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Item
Were any concomitant medications taken by the subject during the study?
text
C2347852 (UMLS CUI [1])
Concomitant Medications
Code List
Were any concomitant medications taken by the subject during the study?
CL Item
Yes (Y)
CL Item
No (N)
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
Dose
Item
Dose
float
C3174092 (UMLS CUI [1])
Units
Item
Units
text
C2826646 (UMLS CUI [1])
Frequency
Item
Frequency
text
C2826654 (UMLS CUI [1])
Route
Item
Route
text
C2826730 (UMLS CUI [1])
Date Started
Item
Date Started
date
C2826734 (UMLS CUI [1])
Pre-study start
Item
Was medication started pre-study?
boolean
C2981448 (UMLS CUI [1])
Date stopped
Item
Date stopped
date
C2826744 (UMLS CUI [1])
Ongoing Medication
Item
Was medication continued post-study?
boolean
C2826666 (UMLS CUI [1])
Conditions treated / Indication
Item
Conditions treated / Indication
text
C2826696 (UMLS CUI [1])
Item
Prophylaxis?
text
C0199176 (UMLS CUI [1])
Prophylaxis
Code List
Prophylaxis?
CL Item
yes (Y)
CL Item
no (N)
Item
Was drug administered for an adverse event?
text
C0877248 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Concomitant Medications
Code List
Was drug administered for an adverse event?
CL Item
Yes (Y)
CL Item
No (N)
Item
Was drug administered as a rescue medication?
text
C0013227 (UMLS CUI [1,1])
C0884980 (UMLS CUI [1,2])
Concomitant Medications
Code List
Was drug administered as a rescue medication?
CL Item
Yes (Y)
CL Item
No (N)
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