ID

33578

Beschrijving

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

Trefwoorden

Versies (3)
  1. 08-11-18 08-11-18 -
  2. 13-12-18 13-12-18 -
  3. 09-01-19 09-01-19 -
Houder van rechten

GSK group of companies

Geüploaded op

13 december 2018

DOI

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Licentie

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

Engels

Session 3: Investigational Product

1 Formulieren  
Administrative data
Beschrijving

Administrative data

Alias
UMLS CUI-1
C1320722
Site
Beschrijving

Site

Datatype

text

Alias
UMLS CUI [1]
C2825164
Patient
Beschrijving

Patient

Datatype

text

Alias
UMLS CUI [1]
C1299487
Patient Number
Beschrijving

Patient Number

Datatype

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1300638
Investigational Product - Regimen A - 40 mg Carvedilol CR
Beschrijving

Investigational Product - Regimen A - 40 mg Carvedilol CR

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1276413
UMLS CUI-3
C0054836
Date of dose
Beschrijving

Date of dose

Datatype

date

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0011008
Time of dose
Beschrijving

Time of dose

Datatype

time

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0040223
Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH
Beschrijving

Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C0054836
UMLS CUI-3
C1276413
UMLS CUI-4
C0001948
Intake Start Date
Beschrijving

Taken together with Carvedilol CR

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0808070
Intake Start Time
Beschrijving

Start Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1301880
Intake Stop Date
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0806020
Intake Stop Time
Beschrijving

Stop Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1522314
Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH
Beschrijving

Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1276413
UMLS CUI-3
C0001948
2.5 Hours before Carvedilol CR
Beschrijving

2.5 Hours before Carvedilol CR

Datatype

text

Intake Start Date
Beschrijving

Start Date

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0808070
Intake Start Time
Beschrijving

Start Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1301880
Intake Stop Date
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0806020
Intake Stop Time
Beschrijving

Stop Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1522314
Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
Beschrijving

Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH

Alias
UMLS CUI-1
C0304229
UMLS CUI-2
C1276413
UMLS CUI-3
C0001948
2 Hours after Cardivelol CR
Beschrijving

2 Hours after Cardivelol CR

Datatype

text

Intake Start Date
Beschrijving

Start Date

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0808070
Intake Start Time
Beschrijving

Start Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1301880
Intake Stop Date
Beschrijving

Stop Date

Datatype

date

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C0806020
Intake Stop Time
Beschrijving

Stop Time

Datatype

time

Alias
UMLS CUI [1,1]
C1512806
UMLS CUI [1,2]
C1522314
Terug naar het begin van de pagina

Similar models

Session 3: Investigational Product

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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
Investigational Product - Regimen A - 40 mg Carvedilol CR
C0304229 (UMLS CUI-1)
C1276413 (UMLS CUI-2)
C0054836 (UMLS CUI-3)
Date of dose
Item
Date of dose
date
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
Time of dose
Item
Time of dose
time
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
Item Group
Investigational Product - 40 mg Carvedilol Regimen B Alcohol Ingestion - 240 ml OF 20%EtOH
C0304229 (UMLS CUI-1)
C0054836 (UMLS CUI-2)
C1276413 (UMLS CUI-3)
C0001948 (UMLS CUI-4)
Start Date
Item
Intake Start Date
date
C1512806 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Start Time
Item
Intake Start Time
time
C1512806 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Stop Date
Item
Intake Stop Date
date
C1512806 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Stop Time
Item
Intake Stop Time
time
C1512806 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Item Group
Investigational Product - Regimen C Alcohol Ingestion - 240 ml OF 20% EtOH
C0304229 (UMLS CUI-1)
C1276413 (UMLS CUI-2)
C0001948 (UMLS CUI-3)
2.5 Hours before Carvedilol CR
Item
2.5 Hours before Carvedilol CR
text
Start Date
Item
Intake Start Date
date
C1512806 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Start Time
Item
Intake Start Time
time
C1512806 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Stop Date
Item
Intake Stop Date
date
C1512806 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Stop Time
Item
Intake Stop Time
time
C1512806 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Item Group
Investigational Product - Regimen D Alcohol Ingestion - 240 ml OF 20% EtOH
C0304229 (UMLS CUI-1)
C1276413 (UMLS CUI-2)
C0001948 (UMLS CUI-3)
2 Hours after Cardivelol CR
Item
2 Hours after Cardivelol CR
text
Start Date
Item
Intake Start Date
date
C1512806 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Start Time
Item
Intake Start Time
time
C1512806 (UMLS CUI [1,1])
C1301880 (UMLS CUI [1,2])
Stop Date
Item
Intake Stop Date
date
C1512806 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
Stop Time
Item
Intake Stop Time
time
C1512806 (UMLS CUI [1,1])
C1522314 (UMLS CUI [1,2])
Terug naar het begin van de pagina 

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