ID

21954

Descrizione

A Double-blind, Randomized, Placebo-controlled, Parallel-group Study to Investigate the Effects of Rosiglitazone (Extended Release Tablets) on Cerebral Glucose Utilization and Cognition in Subjects With Mild to Moderate Alzheimer's Disease (AD) Medicine: rosiglitazone, Condition: Alzheimer's Disease, Phase: 2, Clinical Study ID: 49653/461, Sponsor: GSK Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

collegamento

https://clinicaltrials.gov/ct2/show/NCT00265148?term=NCT00265148&rank=1

Keywords

  1. 09/05/17 09/05/17 -
  2. 22/05/17 22/05/17 -
Caricato su

9 maggio 2017

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 3.0

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ECG Vital Signs A double-blind, randomized, placebo-controlled, parallel-group study to investigate the effects of rosiglitazone (extended release tablets) on cerebral glucose utilization and cognition in subjects with mild to moderate Alzheimer's Disease

ECG Vital Signs A double-blind, randomized, placebo-controlled, parallel-group study to investigate the effects of rosiglitazone (extended release tablets) on cerebral glucose utilization and cognition in subjects with mild to moderate Alzheimer's Disease (AD)

ECG Monitoring
Descrizione

ECG Monitoring

Alias
UMLS CUI-1
C0430456
Date
Descrizione

Date of ECG

Tipo di dati

date

Unità di misura
  • Day Month Year
Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C0013798
Day Month Year
Actual time
Descrizione

Actual time

Tipo di dati

time

Unità di misura
  • Hr : Min
Alias
UMLS CUI [1]
C0040223
Hr : Min
Heart Rate
Descrizione

Heart Rate

Tipo di dati

float

Unità di misura
  • bpm
Alias
UMLS CUI [1]
C0018810
bpm
PR Interval
Descrizione

PR Interval

Tipo di dati

time

Unità di misura
  • msec
Alias
UMLS CUI [1]
C0429087
msec
QRS Duration
Descrizione

QRS Duration

Tipo di dati

time

Unità di misura
  • Hr : Min
Alias
UMLS CUI [1]
C0429025
Hr : Min
Uncorrected QT Interval
Descrizione

Uncorrected QT Interval

Tipo di dati

time

Alias
UMLS CUI [1]
C1287082
QTc interval
Descrizione

QTc interval

Tipo di dati

time

Alias
UMLS CUI [1]
C0489625
Result of the ECG (enter Code for result from following list) *Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) page(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE. Complete the additional ECG Abnormalities page if clinically significant abnormalities are present.
Descrizione

Result of the ECG

Tipo di dati

integer

Alias
UMLS CUI [1]
C0438154

Similar models

ECG Vital Signs A double-blind, randomized, placebo-controlled, parallel-group study to investigate the effects of rosiglitazone (extended release tablets) on cerebral glucose utilization and cognition in subjects with mild to moderate Alzheimer's Disease (AD)

Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
ECG Monitoring
C0430456 (UMLS CUI-1)
Date of ECG
Item
Date
date
C0808070 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
Actual time
Item
Actual time
time
C0040223 (UMLS CUI [1])
Heart Rate
Item
Heart Rate
float
C0018810 (UMLS CUI [1])
PR Interval
Item
PR Interval
time
C0429087 (UMLS CUI [1])
QRS Duration
Item
QRS Duration
time
C0429025 (UMLS CUI [1])
Uncorrected QT Interval
Item
Uncorrected QT Interval
time
C1287082 (UMLS CUI [1])
QTc interval
Item
QTc interval
time
C0489625 (UMLS CUI [1])
Item
Result of the ECG (enter Code for result from following list) *Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) page(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE. Complete the additional ECG Abnormalities page if clinically significant abnormalities are present.
integer
C0438154 (UMLS CUI [1])
Code List
Result of the ECG (enter Code for result from following list) *Complete the Non-Serious Adverse Events (AE) or Serious Adverse Event (SAE) page(s) if clinically significant abnormalities meet the protocol definition for an AE or SAE. Complete the additional ECG Abnormalities page if clinically significant abnormalities are present.
CL Item
Normal (1)
CL Item
Abnormal - not clinically significant (2)
CL Item
Abnormal - clinically significant* (3)
CL Item
No result (not available) (4)

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