ID

28851

Description

Study ID: 100723 Clinical Study ID: AXR100723 Study Title: A 24 Week Randomized, Double-blind, Double-dummy, Multicenter Study to Compare the Efficacy of Formulation X and AVANDIA™ (8mg OD) in Subjects with Type 2 Diabetes Mellitus Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 4 Study Recruitment Status: Completed Generic Name: rosiglitazone Trade Name: Avandia; Avandia XR; Avandia XR,Rosiglitazone XR,Avandia; Rosiglitazone XR Study Indication: Diabetes Mellitus, Type 2 Documentation part: Additional Forms - Medication

Keywords

Versions (1)
  1. 2/8/18 2/8/18 -
Copyright Holder

GlaxoSmithKline

Uploaded on

February 8, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Efficacy of Formulation X and AVANDIA in Subjects with Type 2 Diabetes Mellitus 100723

English

Additional Forms - Medication

1 forms  
Medication
Description

Medication

Alias
UMLS CUI-1
C0013227
Center
Description

Center

Data type

text

Alias
UMLS CUI [1,1]
C1301943
UMLS CUI [1,2]
C0600091
Subject ID
Description

Subject ID

Data type

text

Alias
UMLS CUI [1]
C2348585
Initials
Description

Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Visit Date
Description

Visit Date

Data type

date

Alias
UMLS CUI [1]
C1320303
Drug name (Trade Name preferred)
Description

Drug name

Data type

text

Alias
UMLS CUI [1]
C2360065
Dose
Description

Dose

Data type

float

Alias
UMLS CUI [1]
C3174092
Units
Description

Units

Data type

integer

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C1519795
Frequency
Description

Frequency

Data type

integer

Alias
UMLS CUI [1]
C3476109
Route
Description

Route

Data type

integer

Alias
UMLS CUI [1]
C0013153
Reason for Medication
Description

Reason for Medication

Data type

text

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

Start Date

Data type

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0808070
Ongoing Medication?
Description

Ongoing Medication

Data type

boolean

Alias
UMLS CUI [1]
C2826666
Stop Date
Description

Stop Date

Data type

date

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0806020
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Similar models

Additional Forms - Medication

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Medication
C0013227 (UMLS CUI-1)
Center
Item
Center
text
C1301943 (UMLS CUI [1,1])
C0600091 (UMLS CUI [1,2])
Subject ID
Item
Subject ID
text
C2348585 (UMLS CUI [1])
Initials
Item
Initials
text
C2986440 (UMLS CUI [1])
Visit Date
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Drug name
Item
Drug name (Trade Name preferred)
text
C2360065 (UMLS CUI [1])
Dose
Item
Dose
float
C3174092 (UMLS CUI [1])
Item
Units
integer
C0013227 (UMLS CUI [1,1])
C1519795 (UMLS CUI [1,2])
Units
Code List
Units
CL Item
TAB (1)
CL Item
MCL (2)
CL Item
ML (3)
CL Item
L (4)
CL Item
MCG (5)
CL Item
MG (6)
CL Item
G (7)
Item
Frequency
integer
C3476109 (UMLS CUI [1])
Frequency
Code List
Frequency
CL Item
OD/QD (1)
CL Item
BID (2)
CL Item
TID (3)
CL Item
QID (4)
CL Item
PRN (5)
CL Item
QOD (6)
CL Item
WKY (7)
CL Item
2XWK (8)
CL Item
3XWK (9)
CL Item
Other (10)
CL Item
Unknown (11)
Item
Route
integer
C0013153 (UMLS CUI [1])
Route
Code List
Route
CL Item
Oral (1)
CL Item
Intravenous (2)
CL Item
Intramuscular (3)
CL Item
Intra-arterial (4)
CL Item
Topical (5)
CL Item
Sublingual (6)
CL Item
Intrathecal (7)
CL Item
Vaginal (8)
CL Item
Nasal (9)
CL Item
Intra-articular injection (10)
CL Item
Transdermal (11)
CL Item
Inhalation (12)
CL Item
Subcutaneous (13)
CL Item
Rectal (14)
CL Item
Intradermal (15)
CL Item
Intralesion (16)
CL Item
Intraperitoneal (17)
CL Item
Other (18)
CL Item
Unknown (19)
Reason for Medication
Item
Reason for Medication
text
C0013227 (UMLS CUI [1,1])
C0392360 (UMLS CUI [1,2])
Start Date
Item
Start Date
date
C0013227 (UMLS CUI [1,1])
C0808070 (UMLS CUI [1,2])
Ongoing Medication
Item
Ongoing Medication?
boolean
C2826666 (UMLS CUI [1])
Stop Date
Item
Stop Date
date
C0013227 (UMLS CUI [1,1])
C0806020 (UMLS CUI [1,2])
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