ID

20496

Beschreibung

The purpose of the trial is to determine if extended-release dipyridamole + aspirin [Aggrenox, Asasa ntin] is superior to clopidogrel [Plavix], and if telmisartan [Micardis, Gliosartan, Kinzal, Kinzalm ono, Predxal, Pritor, Samertan, Telmisartan] is superior to placebo, in the presence of background antihypertensive therapy, in prevention of a second stroke in patients who have recently suffered a stroke and therefore are at high risk of suffering another one. Source & Descriptions: https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Link

https://clinicaltrials.gov/ct2/show/NCT00153062?term=NCT00153062&rank=1

Stichworte

  1. 27.02.17 27.02.17 -
Hochgeladen am

27. Februar 2017

DOI

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Medical History Visit 1 Month 0 PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Medical History Visit 1 Month 0 PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Medical History
Beschreibung

Medical History

Alias
UMLS CUI-1
C0262926
1. Number of Previous Symptomatic Strokes (not including qualifying stroke)
Beschreibung

Number of Previous Symptomatic Strokes

Datentyp

float

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0750480
Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (2)
Beschreibung

Date of recent Stroke

Datentyp

date

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0750480
2. Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (1)
Beschreibung

Date of recent stroke

Datentyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0038454
Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (3)
Beschreibung

Date of recent Stroke

Datentyp

date

Alias
UMLS CUI [1,1]
C0038454
UMLS CUI [1,2]
C0750480
Does the patient have any of the following:
Beschreibung

Does the patient have any of the following:

Alias
UMLS CUI-1
C0011900
UMLS CUI-2
C0205394
3. Ischemic coronary artery disease
Beschreibung

Ischemic coronary artery disease

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1956346
UMLS CUI [1,2]
C0151744
UMLS CUI [1,3]
C0262926
if "yes", year of first diagnosis
Beschreibung

if "yes", year of first diagnosis

Datentyp

date

Alias
UMLS CUI [1,1]
C0205265
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0439234
UMLS CUI [1,4]
C0151744
4. Prior myocardial infarctions
Beschreibung

Prior myocardial infarctions

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0262926
if "yes", number of infarctions
Beschreibung

if "yes", number of infarctions

Datentyp

float

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0750480
if "yes", date of most recent infarctions
Beschreibung

if "yes", date of most recent infarctions

Datentyp

date

Alias
UMLS CUI [1,1]
C0027051
UMLS CUI [1,2]
C0011008
5. Peripheral arterial occlusive disease (PAOD)
Beschreibung

Peripheral arterial occlusive disease (PAOD)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1306889
UMLS CUI [1,2]
C0262926
if "yes", year of first diagnosis (yy)
Beschreibung

if "yes", year of first diagnosis (yy)

Datentyp

date

Alias
UMLS CUI [1,1]
C0205265
UMLS CUI [1,2]
C0011900
UMLS CUI [1,3]
C0439234
UMLS CUI [1,4]
C1306889
6. Prior Transient Ischemic Attacks
Beschreibung

Prior Transient Ischemic Attacks

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007787
UMLS CUI [1,2]
C0262926
if ´yes´, Date of last Transient Ischemic Attack
Beschreibung

if ´yes´, Date of last TIA

Datentyp

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C0007787
7. Diabetes mellitus
Beschreibung

Diabetes mellitus

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0011849
UMLS CUI [1,2]
C0262926
if ´yes´, age at of diagnosis (years)
Beschreibung

if ´yes´, age at of diagnosis

Datentyp

date

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0205265
UMLS CUI [1,3]
C0011900
8. Hypertension
Beschreibung

Hypertension

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C0262926
if ´yes´, age at diagnosis (years)
Beschreibung

if ´yes´, age at diagnosis

Datentyp

date

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C0205265
UMLS CUI [1,3]
C0011900
9. Hyperlipidemia
Beschreibung

Hyperlipidemia

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020473
UMLS CUI [1,2]
C0262926
10. Atrial fibrillation
Beschreibung

Atrial fibrillation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0004238
UMLS CUI [1,2]
C0262926
11. Congestive Heart failure (CHF)
Beschreibung

Congestive Heart failure (CHF)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C0262926
12. Deep venous thrombosis (DVT)
Beschreibung

Deep venous thrombosis (DVT)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0149871
UMLS CUI [1,2]
C0262926
13. Valvular disease
Beschreibung

Valvular disease

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3258293
UMLS CUI [1,2]
C0262926
14. Did the patient suffer from migraine headaches in the last 12 months.
Beschreibung

Migraine headaches

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0149931
UMLS CUI [1,2]
C0262926
if ´no´, has the patient previously suffered from migraine headaches (<10 attacks/lifetime)
Beschreibung

if ´no´, has the patient previously suffered from migraine headaches (<10 attacks/lifetime)

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0149931
UMLS CUI [1,2]
C4071830
UMLS CUI [1,3]
C0262926
Laboratory Blood Tests
Beschreibung

Laboratory Blood Tests

Alias
UMLS CUI-1
C0018941
15. Has a laboratory test been performed? (results from previous 3 month are acceptable)
Beschreibung

Laboratory Blood Test Performance

Datentyp

boolean

Alias
UMLS CUI [1]
C2346633
If Yes, date of sample
Beschreibung

Date

Datentyp

date

Alias
UMLS CUI [1,1]
C2346633
UMLS CUI [1,2]
C0011008
16. Potassium Value (and Unit)
Beschreibung

Potassium Value

Datentyp

float

Alias
UMLS CUI [1]
C0556596
17. Creatinine Value (and Unit)
Beschreibung

Creatinine Value

Datentyp

float

Alias
UMLS CUI [1]
C0201975
Optional tests (No new test should be performed to obtain results)
Beschreibung

Optional tests (No new test should be performed to obtain results)

Alias
UMLS CUI-1
C0392366
18. White Blood Cell Count Value
Beschreibung

White Blood Cell Count Value

Datentyp

float

Alias
UMLS CUI [1]
C0023508
19. Haematocrit Value
Beschreibung

Haematocrit

Datentyp

float

Alias
UMLS CUI [1]
C0018935

Ähnliche Modelle

Medical History Visit 1 Month 0 PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Medical History
C0262926 (UMLS CUI-1)
Number of Previous Symptomatic Strokes
Item
1. Number of Previous Symptomatic Strokes (not including qualifying stroke)
float
C0038454 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Date of recent Stroke
Item
Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (2)
date
C0038454 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Date of recent stroke
Item
2. Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (1)
date
C0011008 (UMLS CUI [1,1])
C0038454 (UMLS CUI [1,2])
Date of recent Stroke
Item
Date of most recent prior Strokes (not including qualifying stroke) (dd mon yy): (Starting with most recent) (3)
date
C0038454 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
Item Group
Does the patient have any of the following:
C0011900 (UMLS CUI-1)
C0205394 (UMLS CUI-2)
Ischemic coronary artery disease
Item
3. Ischemic coronary artery disease
boolean
C1956346 (UMLS CUI [1,1])
C0151744 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
if "yes", year of first diagnosis
Item
if "yes", year of first diagnosis
date
C0205265 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0439234 (UMLS CUI [1,3])
C0151744 (UMLS CUI [1,4])
Prior myocardial infarctions
Item
4. Prior myocardial infarctions
boolean
C0027051 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if "yes", number of infarctions
Item
if "yes", number of infarctions
float
C0027051 (UMLS CUI [1,1])
C0750480 (UMLS CUI [1,2])
if "yes", date of most recent infarctions
Item
if "yes", date of most recent infarctions
date
C0027051 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Peripheral arterial occlusive disease (PAOD)
Item
5. Peripheral arterial occlusive disease (PAOD)
boolean
C1306889 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if "yes", year of first diagnosis (yy)
Item
if "yes", year of first diagnosis (yy)
date
C0205265 (UMLS CUI [1,1])
C0011900 (UMLS CUI [1,2])
C0439234 (UMLS CUI [1,3])
C1306889 (UMLS CUI [1,4])
Prior Transient Ischemic Attacks
Item
6. Prior Transient Ischemic Attacks
boolean
C0007787 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if ´yes´, Date of last TIA
Item
if ´yes´, Date of last Transient Ischemic Attack
date
C0011008 (UMLS CUI [1,1])
C0007787 (UMLS CUI [1,2])
Diabetes mellitus
Item
7. Diabetes mellitus
boolean
C0011849 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if ´yes´, age at of diagnosis
Item
if ´yes´, age at of diagnosis (years)
date
C0001779 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
Hypertension
Item
8. Hypertension
boolean
C0020538 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if ´yes´, age at diagnosis
Item
if ´yes´, age at diagnosis (years)
date
C0001779 (UMLS CUI [1,1])
C0205265 (UMLS CUI [1,2])
C0011900 (UMLS CUI [1,3])
Hyperlipidemia
Item
9. Hyperlipidemia
boolean
C0020473 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Atrial fibrillation
Item
10. Atrial fibrillation
boolean
C0004238 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Congestive Heart failure (CHF)
Item
11. Congestive Heart failure (CHF)
boolean
C0018802 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Deep venous thrombosis (DVT)
Item
12. Deep venous thrombosis (DVT)
boolean
C0149871 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Valvular disease
Item
13. Valvular disease
boolean
C3258293 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
Migraine headaches
Item
14. Did the patient suffer from migraine headaches in the last 12 months.
boolean
C0149931 (UMLS CUI [1,1])
C0262926 (UMLS CUI [1,2])
if ´no´, has the patient previously suffered from migraine headaches (<10 attacks/lifetime)
Item
if ´no´, has the patient previously suffered from migraine headaches (<10 attacks/lifetime)
boolean
C0149931 (UMLS CUI [1,1])
C4071830 (UMLS CUI [1,2])
C0262926 (UMLS CUI [1,3])
Item Group
Laboratory Blood Tests
C0018941 (UMLS CUI-1)
Laboratory Blood Test Performance
Item
15. Has a laboratory test been performed? (results from previous 3 month are acceptable)
boolean
C2346633 (UMLS CUI [1])
Date
Item
If Yes, date of sample
date
C2346633 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Potassium Value
Item
16. Potassium Value (and Unit)
float
C0556596 (UMLS CUI [1])
Creatinine Value
Item
17. Creatinine Value (and Unit)
float
C0201975 (UMLS CUI [1])
Item Group
Optional tests (No new test should be performed to obtain results)
C0392366 (UMLS CUI-1)
White Blood Cell Count Value
Item
18. White Blood Cell Count Value
float
C0023508 (UMLS CUI [1])
Haematocrit
Item
19. Haematocrit Value
float
C0018935 (UMLS CUI [1])

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