ID

30556

Beskrivning

https://clinicaltrials.gov/ct2/show/NCT00344006 Study ID : CDA 714703/005 Clinical Study ID :714703/005 Study Title :A multi-centre, randomised, double-blind, double dummy study comparing the efficacy and safety of chlorproguanil-dapsone-artesunate versus artemether-lumefantrine in the treatment of acute uncomplicated Plasmodium falciparum malaria in children and adolescents in Africa. Patient Level Data : Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier : NCT00344006 Sponsor : GlaxoSmithKline Collaborators : N/A Phase phase :3 Study Recruitment Status : Completed Generic Name : artesunate/chlorproguanil/dapsone Trade Name : LAPDAP + ARTESUNATE Study Indication : Malaria, Falciparum

Länk

https://clinicaltrials.gov/ct2/show/NCT00344006

Nyckelord

Versioner (1)
  1. 2018-06-14 2018-06-14 - Halim Ugurlu
Rättsinnehavare

GlaxoSmithKline (GSK)

Uppladdad den

14 juni 2018

DOI

För en begäran logga in.

Licens

Creative Commons BY-NC 3.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

NCT00344006-Chlorproguanil-Dapsone-Artesunate Versus COARTEM For Uncomplicated Malaria

Engelsk

Case Report From, Module Number 2.1 (Concominant Medications, Anti-Malarial Rescue Concominant Medications)

1 Formulär  
Administrative Information
Beskrivning

Administrative Information

Alias
UMLS CUI-1
C1320722
Subject Identifier
Beskrivning

Subject Identifier

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Visit Date
Beskrivning

Visit Date

Datatyp

date

Alias
UMLS CUI [1]
C1320303
Concominant Medications
Beskrivning

Concominant Medications

Alias
UMLS CUI-1
C2347852
Were any concominant medications taken by the subject prior to screening and/or during the study?
Beskrivning

concominant medications

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2826257
UMLS CUI [1,2]
C2347852
Concominant Medications
Beskrivning

Concominant Medications

Alias
UMLS CUI-1
C2347852
Drug Name
Beskrivning

Drug Name

Datatyp

text

Alias
UMLS CUI [1]
C2360065
Unit Dose
Beskrivning

Unit Dose

Datatyp

float

Alias
UMLS CUI [1]
C0869039
Units
Beskrivning

Units

Datatyp

text

Alias
UMLS CUI [1]
C0439148
Frequency
Beskrivning

Frequency

Datatyp

text

Alias
UMLS CUI [1]
C3476109
Route
Beskrivning

Route

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Reason for medication
Beskrivning

Reason for medication

Datatyp

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date
Beskrivning

Start Date

Datatyp

date

Alias
UMLS CUI [1]
C0808070
Start Time
Beskrivning

Start Time

Datatyp

time

Alias
UMLS CUI [1]
C1301880
Taken prior to study?
Beskrivning

Taken prior to study

Datatyp

boolean

Alias
UMLS CUI [1]
C2826667
Stop Date
Beskrivning

Stop Date

Datatyp

date

Alias
UMLS CUI [1]
C0806020
Stop Time
Beskrivning

Stop Time

Datatyp

time

Alias
UMLS CUI [1]
C1522314
Ongoing Medication?
Beskrivning

Ongoing Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
Anti-Malarial Rescue Concominant Medications
Beskrivning

Anti-Malarial Rescue Concominant Medications

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C2193813
Were any anti-malarial concominant medications taken by the subject during the study?
Beskrivning

anti-malarial concominant medications

Datatyp

boolean

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C2193813
Anti-Malarial Rescue Concominant Medications
Beskrivning

Anti-Malarial Rescue Concominant Medications

Alias
UMLS CUI-1
C2347852
UMLS CUI-2
C2193813
Drug Name
Beskrivning

Drug Name

Datatyp

text

Alias
UMLS CUI [1]
C2360065
Unit Dose
Beskrivning

Unit Dose

Datatyp

float

Alias
UMLS CUI [1]
C0869039
Units
Beskrivning

Units

Datatyp

text

Alias
UMLS CUI [1]
C0439148
Frequency
Beskrivning

Frequency

Datatyp

text

Alias
UMLS CUI [1]
C3476109
Route
Beskrivning

Route

Datatyp

text

Alias
UMLS CUI [1]
C0013153
Reason for medication
Beskrivning

Reason for medication

Datatyp

text

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0013227
Start Date
Beskrivning

Start Date

Datatyp

date

Alias
UMLS CUI [1]
C0808070
Start Time
Beskrivning

Start Time

Datatyp

time

Alias
UMLS CUI [1]
C1301880
Stop Date
Beskrivning

Stop Date

Datatyp

date

Alias
UMLS CUI [1]
C0806020
Stop Time
Beskrivning

Stop Time

Datatyp

time

Alias
UMLS CUI [1]
C1522314
Ongoing Medication?
Beskrivning

Ongoing Medication

Datatyp

boolean

Alias
UMLS CUI [1]
C2826666
Tillbaka till toppen

Similar models

Case Report From, Module Number 2.1 (Concominant Medications, Anti-Malarial Rescue Concominant Medications)

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative Information
C1320722 (UMLS CUI-1)
Subject Identifier
Item
Subject Identifier
text
C2348585 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Item Group
Concominant Medications
C2347852 (UMLS CUI-1)
concominant medications
Item
Were any concominant medications taken by the subject prior to screening and/or during the study?
boolean
C2826257 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item Group
Concominant Medications
C2347852 (UMLS CUI-1)
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
Unit Dose
Item
Unit Dose
float
C0869039 (UMLS CUI [1])
Units
Item
Units
text
C0439148 (UMLS CUI [1])
Frequency
Item
Frequency
text
C3476109 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Reason for medication
Item
Reason for medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Start Time
Item
Start Time
time
C1301880 (UMLS CUI [1])
Taken prior to study
Item
Taken prior to study?
boolean
C2826667 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Stop Time
Item
Stop Time
time
C1522314 (UMLS CUI [1])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])
Item Group
Anti-Malarial Rescue Concominant Medications
C2347852 (UMLS CUI-1)
C2193813 (UMLS CUI-2)
anti-malarial concominant medications
Item
Were any anti-malarial concominant medications taken by the subject during the study?
boolean
C2347852 (UMLS CUI [1,1])
C2193813 (UMLS CUI [1,2])
Item Group
Anti-Malarial Rescue Concominant Medications
C2347852 (UMLS CUI-1)
C2193813 (UMLS CUI-2)
Drug Name
Item
Drug Name
text
C2360065 (UMLS CUI [1])
Unit Dose
Item
Unit Dose
float
C0869039 (UMLS CUI [1])
Units
Item
Units
text
C0439148 (UMLS CUI [1])
Frequency
Item
Frequency
text
C3476109 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Reason for medication
Item
Reason for medication
text
C0392360 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0808070 (UMLS CUI [1])
Start Time
Item
Start Time
time
C1301880 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0806020 (UMLS CUI [1])
Stop Time
Item
Stop Time
time
C1522314 (UMLS CUI [1])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial