ID

34030

Descripción

Study ID: 106904 Clinical Study ID: CRV106904 Study Title: A Randomized, Open-Label, Single-Dose, Four-Period Cross-Over Study to Determine the Effects of Alcohol on the Pharmacokinetics of Carvedilol CR Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: carvedilol Trade Name: Coreg CR,Coreg Study Indication: Hypertension

Palabras clave

Versiones (2)
  1. 9/11/18 9/11/18 -
  2. 11/1/19 11/1/19 -
Titular de derechos de autor

GSK group of companies

Subido en

11 de enero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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A Cross-Over Study of Alcohol Effect on the Pharmacokinetics of Carvedilol - 106904

Inglés

Logs and Repeats: Concomitant Medications

1 formularios  
Administrative data
Descripción

Administrative data

Alias
UMLS CUI-1
C1320722
Site
Descripción

Site

Tipo de datos

text

Alias
UMLS CUI [1]
C2825164
Patient
Descripción

Patient

Tipo de datos

text

Alias
UMLS CUI [1]
C1299487
Patient Number
Descripción

Patient Number

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1300638
Concomitant Medications
Descripción

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Sequence Number
Descripción

Sequence Number

Tipo de datos

integer

Alias
UMLS CUI [1]
C2348184
Drug name
Descripción

Trade name preferred

Tipo de datos

text

Alias
UMLS CUI [1]
C0013227
Modified reported term
Descripción

Modified reported term

Tipo de datos

text

Alias
UMLS CUI [1]
C2826819
Unit dose
Descripción

Unit dose

Tipo de datos

float

Alias
UMLS CUI [1]
C0869039
Units
Descripción

Units

Tipo de datos

text

Alias
UMLS CUI [1]
C1519795
Frequency
Descripción

Frequency

Tipo de datos

integer

Alias
UMLS CUI [1]
C3476109
Route
Descripción

Route

Tipo de datos

text

Alias
UMLS CUI [1]
C0013153
Reason for medication
Descripción

Reason for medication

Tipo de datos

text

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

Start Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0808070
Start Time
Descripción

Start Time

Tipo de datos

time

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

Taken prior to study?

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2826667
Ongoing?
Descripción

Ongoing?

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2826666
If NO, record End Date
Descripción

If NO, record End Date

Tipo de datos

date

Alias
UMLS CUI [1]
C0806020
If NO, record End Time
Descripción

If NO, record End Time

Tipo de datos

time

Alias
UMLS CUI [1]
C1522314
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Similar models

Logs and Repeats: Concomitant Medications

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Administrative data
C1320722 (UMLS CUI-1)
Site
Item
Site
text
C2825164 (UMLS CUI [1])
Patient
Item
Patient
text
C1299487 (UMLS CUI [1])
Patient Number
Item
Patient Number
integer
C0030705 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Sequence Number
Item
Sequence Number
integer
C2348184 (UMLS CUI [1])
Drug name
Item
Drug name
text
C0013227 (UMLS CUI [1])
Modified reported term
Item
Modified reported term
text
C2826819 (UMLS CUI [1])
Unit dose
Item
Unit dose
float
C0869039 (UMLS CUI [1])
Units
Item
Units
text
C1519795 (UMLS CUI [1])
Frequency
Item
Frequency
integer
C3476109 (UMLS CUI [1])
Route
Item
Route
text
C0013153 (UMLS CUI [1])
Reason for medication
Item
Reason for medication
text
C0013227 (UMLS CUI [1,1])
C0392360 (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])
Ongoing?
Item
Ongoing?
boolean
C2826666 (UMLS CUI [1])
If NO, record End Date
Item
If NO, record End Date
date
C0806020 (UMLS CUI [1])
If NO, record End Time
Item
If NO, record End Time
time
C1522314 (UMLS CUI [1])
Volver a la parte superior de la página 

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