ID

32006

Beskrivning

Study ID: 105-040 Clinical Study ID: 105-040 Study Title: A Multicenter, Double-Blind, Placebo-Controlled, Parallel-Design Evaluation of LAMICTAL for Add-on Treatment of Partial Seizures in Pediatric Patients Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: lamotrigine Trade Name: lamictal Study Indication: Epilepsy, Partial

Nyckelord

Versioner (6)
  1. 2018-09-21 2018-09-21 -
  2. 2018-09-22 2018-09-22 -
  3. 2018-09-22 2018-09-22 -
  4. 2018-09-27 2018-09-27 -
  5. 2018-10-08 2018-10-08 -
  6. 2018-10-11 2018-10-11 -
Rättsinnehavare

GlaxoSmithKline

Uppladdad den

11 oktober 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.

Evaluation of LAMICTAL for Add-on Treatment of Partial Seizures in Pediatric Patients 105-040

Engelsk

Concomitant Medications - Study Week 1 Through Taper and Follow- up, AED Prescription and Compliance - Week 2 through Taper and Follow- Up, Study Medication Prescription and Compliance Record - Study Week 9 Through Taper and Follow- Up

1 Formulär  
Administrative
Beskrivning

Administrative

Alias
UMLS CUI-1
C1320722
Site number
Beskrivning

Study Site; Numbers

Datatyp

text

Alias
UMLS CUI [1,1]
C2825164
UMLS CUI [1,2]
C0237753
Patient's initials
Beskrivning

Person Initials

Datatyp

text

Alias
UMLS CUI [1]
C2986440
Patient's trial number
Beskrivning

Clinical Trial Subject Unique Identifier

Datatyp

text

Alias
UMLS CUI [1]
C2348585
Additional medications
Beskrivning

Additional medications

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C1706712
Were any additional medications other than antiepileptic drugs taken during the study? (If yes, record below.)
Beskrivning

Pharmaceutical Preparations; Additional Therapy; Taken; Clinical Trials; During

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1706712
UMLS CUI [1,3]
C1883727
UMLS CUI [1,4]
C0008976
UMLS CUI [1,5]
C0347984
Record Additional medications
Beskrivning

Record Additional medications

Alias
UMLS CUI-1
C0013227
UMLS CUI-2
C1706712
UMLS CUI-3
C0034869
Date medication first taken during study
Beskrivning

Date in time; Pharmaceutical Preparations; Taken

Datatyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C1883727
Name of drug/ Generic
Beskrivning

Medication name | Generic drug name

Datatyp

text

Alias
UMLS CUI [1]
C2360065
UMLS CUI [2]
C0592502
AED Prescription Record
Beskrivning

AED Prescription Record

Alias
UMLS CUI-1
C0003299
UMLS CUI-2
C1521941
Name of antiepileptic drug
Beskrivning

Antiepileptic Agents; Medication name

Datatyp

text

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C2360065
Start date antiepileptic drug
Beskrivning

Antiepileptic Agents; Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0808070
Stop date antiepileptic drug
Beskrivning

Antiepileptic Agents; End date

Datatyp

text

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0806020
Time of dose 1
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 1
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 2
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 2
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 3
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 3
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 4
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 4
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 5
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 5
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Antiepileptic drugs Compliance Record
Beskrivning

Antiepileptic drugs Compliance Record

Alias
UMLS CUI-1
C0003299
UMLS CUI-2
C0525058
Name of antiepileptic drug
Beskrivning

Antiepileptic Agents; Medication name

Datatyp

text

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C2360065
Start date antiepileptic drug
Beskrivning

Antiepileptic Agents; Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0808070
Stop date antiepileptic drug
Beskrivning

Antiepileptic Agents; End date

Datatyp

date

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0806020
Time of dose 1
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 1
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 2
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 2
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 3
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 3
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 4
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 4
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 5
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 5
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
AED entire day's dosing information
Beskrivning

AED entire day's dosing information

Alias
UMLS CUI-1
C0003299
UMLS CUI-2
C0678766
UMLS CUI-3
C1533716
UMLS CUI-4
C0439228
UMLS CUI-5
C0439751
Name of antiepileptic drug
Beskrivning

Antiepileptic Agents; Medication name

Datatyp

text

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C2360065
Start date antiepileptic drug
Beskrivning

Antiepileptic Agents; Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0808070
Stop date antiepileptic drug
Beskrivning

Antiepileptic Agents; End date

Datatyp

date

Alias
UMLS CUI [1,1]
C0003299
UMLS CUI [1,2]
C0806020
Time of dose 1
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 1
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 2
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 2
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 3
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 3
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 4
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 4
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Time of dose 5
Beskrivning

Dosage; Time

Datatyp

time

Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0040223
Amount of dose 5
Beskrivning

Dosage

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1]
C0178602
mg
Study Medication Prescription Record
Beskrivning

Study Medication Prescription Record

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1521941
Study Medication Start date
Beskrivning

Experimental drug; Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0808070
Study Medication Stop Date
Beskrivning

Experimental drug; End Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0806020
Protocol required scheduled dose
Beskrivning

Dosage; Schedule (document type); Study Protocol; Requirement

Datatyp

float

Måttenheter
  • mg/kg/day
Alias
UMLS CUI [1,1]
C0178602
UMLS CUI [1,2]
C0086960
UMLS CUI [1,3]
C2348563
UMLS CUI [1,4]
C1514873
mg/kg/day
Weight
Beskrivning

Body Weight

Datatyp

float

Måttenheter
  • kg
Alias
UMLS CUI [1]
C0005910
kg
Calculated dose
Beskrivning

Medication dose; Calculated

Datatyp

text

Måttenheter
  • mg/day
Alias
UMLS CUI [1,1]
C3174092
UMLS CUI [1,2]
C0444686
mg/day
Investigator actual prescribed dose - A.M. dose - Time
Beskrivning

Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; a.m.

Datatyp

time

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0278329
UMLS CUI [1,3]
C0008961
UMLS CUI [2,1]
C0304229
UMLS CUI [2,2]
C0040223
UMLS CUI [2,3]
C4331833
Investigator actual prescribed dose - A.M. dose - Amount
Beskrivning

Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; a.m.

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0278329
UMLS CUI [1,3]
C0008961
UMLS CUI [2,1]
C0304229
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C4331833
mg
Investigator actual prescribed dose - P.M. dose - Time
Beskrivning

Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; post meridiem

Datatyp

time

Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0278329
UMLS CUI [1,3]
C0008961
UMLS CUI [2,1]
C0304229
UMLS CUI [2,2]
C0040223
UMLS CUI [2,3]
C1509133
Investigator actual prescribed dose - P.M. dose - Amount
Beskrivning

Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; post meridiem

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C0678766
UMLS CUI [1,2]
C0278329
UMLS CUI [1,3]
C0008961
UMLS CUI [2,1]
C0304229
UMLS CUI [2,2]
C0178602
UMLS CUI [2,3]
C1509133
mg
Study Medication Compliance Record
Beskrivning

Study Medication Compliance Record

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C3714738
UMLS CUI-3
C0034869
Study Medication Start date
Beskrivning

Experimental drug; Start Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0808070
Study Medication Stop Date
Beskrivning

Experimental drug; End Date

Datatyp

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0806020
A.M. dose - Amount of dose
Beskrivning

Experimental drug; Dosage; a.m.

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C4331833
mg
A.M. dose - Time
Beskrivning

Experimental drug; Time; a.m.

Datatyp

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0040223
UMLS CUI [1,3]
C4331833
P.M. dose - Amount of dose
Beskrivning

Experimental drug; Dosage; post meridiem

Datatyp

float

Måttenheter
  • mg
Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1509133
mg
P.M. dose - Time
Beskrivning

Experimental drug; Time; post meridiem

Datatyp

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0040223
UMLS CUI [1,3]
C1509133
Tillbaka till toppen

Similar models

Concomitant Medications - Study Week 1 Through Taper and Follow- up, AED Prescription and Compliance - Week 2 through Taper and Follow- Up, Study Medication Prescription and Compliance Record - Study Week 9 Through Taper and Follow- Up

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Administrative
C1320722 (UMLS CUI-1)
Study Site; Numbers
Item
Site number
text
C2825164 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Person Initials
Item
Patient's initials
text
C2986440 (UMLS CUI [1])
Clinical Trial Subject Unique Identifier
Item
Patient's trial number
text
C2348585 (UMLS CUI [1])
Item Group
Additional medications
C0013227 (UMLS CUI-1)
C1706712 (UMLS CUI-2)
Pharmaceutical Preparations; Additional Therapy; Taken; Clinical Trials; During
Item
Were any additional medications other than antiepileptic drugs taken during the study? (If yes, record below.)
boolean
C0013227 (UMLS CUI [1,1])
C1706712 (UMLS CUI [1,2])
C1883727 (UMLS CUI [1,3])
C0008976 (UMLS CUI [1,4])
C0347984 (UMLS CUI [1,5])
Item Group
Record Additional medications
C0013227 (UMLS CUI-1)
C1706712 (UMLS CUI-2)
C0034869 (UMLS CUI-3)
Date in time; Pharmaceutical Preparations; Taken
Item
Date medication first taken during study
date
C0011008 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C1883727 (UMLS CUI [1,3])
Medication name | Generic drug name
Item
Name of drug/ Generic
text
C2360065 (UMLS CUI [1])
C0592502 (UMLS CUI [2])
Item Group
AED Prescription Record
C0003299 (UMLS CUI-1)
C1521941 (UMLS CUI-2)
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Item Group
Antiepileptic drugs Compliance Record
C0003299 (UMLS CUI-1)
C0525058 (UMLS CUI-2)
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Item Group
AED entire day's dosing information
C0003299 (UMLS CUI-1)
C0678766 (UMLS CUI-2)
C1533716 (UMLS CUI-3)
C0439228 (UMLS CUI-4)
C0439751 (UMLS CUI-5)
Antiepileptic Agents; Medication name
Item
Name of antiepileptic drug
text
C0003299 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Antiepileptic Agents; Start Date
Item
Start date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Antiepileptic Agents; End date
Item
Stop date antiepileptic drug
date
C0003299 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Time
Item
Time of dose 1
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 1
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 2
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 2
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 3
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 3
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 4
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 4
float
C0178602 (UMLS CUI [1])
Dosage; Time
Item
Time of dose 5
time
C0178602 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Dosage
Item
Amount of dose 5
float
C0178602 (UMLS CUI [1])
Item Group
Study Medication Prescription Record
C0304229 (UMLS CUI-1)
C1521941 (UMLS CUI-2)
Experimental drug; Start Date
Item
Study Medication Start date
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Experimental drug; End Date
Item
Study Medication Stop Date
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Dosage; Schedule (document type); Study Protocol; Requirement
Item
Protocol required scheduled dose
float
C0178602 (UMLS CUI [1,1])
C0086960 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C1514873 (UMLS CUI [1,4])
Body Weight
Item
Weight
float
C0005910 (UMLS CUI [1])
Medication dose; Calculated
Item
Calculated dose
text
C3174092 (UMLS CUI [1,1])
C0444686 (UMLS CUI [1,2])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; a.m.
Item
Investigator actual prescribed dose - A.M. dose - Time
time
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C4331833 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; a.m.
Item
Investigator actual prescribed dose - A.M. dose - Amount
float
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C4331833 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Time; post meridiem
Item
Investigator actual prescribed dose - P.M. dose - Time
time
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0040223 (UMLS CUI [2,2])
C1509133 (UMLS CUI [2,3])
Drug dose; prescribed; Clinical Investigators; |Experimental drug; Dosage; post meridiem
Item
Investigator actual prescribed dose - P.M. dose - Amount
float
C0678766 (UMLS CUI [1,1])
C0278329 (UMLS CUI [1,2])
C0008961 (UMLS CUI [1,3])
C0304229 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C1509133 (UMLS CUI [2,3])
Item Group
Study Medication Compliance Record
C0304229 (UMLS CUI-1)
C3714738 (UMLS CUI-2)
C0034869 (UMLS CUI-3)
Experimental drug; Start Date
Item
Study Medication Start date
date
C0304229 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Experimental drug; End Date
Item
Study Medication Stop Date
date
C0304229 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Experimental drug; Dosage; a.m.
Item
A.M. dose - Amount of dose
float
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C4331833 (UMLS CUI [1,3])
Experimental drug; Time; a.m.
Item
A.M. dose - Time
time
C0304229 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C4331833 (UMLS CUI [1,3])
Experimental drug; Dosage; post meridiem
Item
P.M. dose - Amount of dose
float
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1509133 (UMLS CUI [1,3])
Experimental drug; Time; post meridiem
Item
P.M. dose - Time
time
C0304229 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
C1509133 (UMLS CUI [1,3])
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