ID

13670

Description

Coronary Artery Bypass graft surgery in patients with Asymptomatic Carotid Stenosis. A randomized controlled clinical trial. Short title: "CABACS" DRKS Number:DRKS00000521 IRSCTN Number:ISRCTN13486906 Phase:Therapeutic confirmatory(Phase III) Head of clinical trial: Prof. Dr. med. Christian Weimar University Duisburg-Essen Phone: 0201/723-6503 Fax: 0201/723-6948 e-mail: christian.weimar@uk-essen.de University Hospital Essen Hospital for Neurology Hufelandstr. 55 45122 Essen Trial coordinator: Dr. med. Stephan Knipp Phone: 0201/723-4915 Fax: 0201/723-5451 e-mail: stephan.knipp@uk-essen.de University Duisburg-Essen University Hospital Essen Hospital for thoracic- and cardiovascular surgery Hufelandstr. 55 45122 Essen Data Management: Anja Marr Phone: 0201/92239-257 Fax: 0201/92239-333 o. 0201/723-5933 e-mail: anja.marr@uk-essen.de University Hospital Essen Center for clinical trials Essen c/o IMIBE Hufelandstr. 55 45122 Essen Monitoring: Dipl.-Biol. Konstantinos Bilbilis Phone: 0201/92239-252 Fax: 0201/92239-310 e-mail: konstantinos.bilbilis@uk-essen.de University Hospital Essen Center for clinical trials Essen c/o IMIBE Hufelandstr. 55 45122 Essen

Keywords

Versions (2)
  1. 2/26/16 2/26/16 -
  2. 9/20/21 9/20/21 -
Uploaded on

February 26, 2016

DOI

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License

Creative Commons BY-NC 3.0
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Baseline visit Coronary Artery Bypass graft surgery in patients with Asymptomatic Carotid Stenosis DRKS00000521

English

CABACS Case Report Form [Baseline visit]

1 forms  
Baseline Examination
Description

Baseline Examination

Date of visit
Description

Date

Data type

date

Alias
UMLS CUI [1]
C0011008
Patient ID
Description

Patient Study ID

Data type

text

Alias
UMLS CUI [1]
C2348585
ECG done?
Description

ECG

Data type

boolean

Alias
UMLS CUI [1]
C1623258
Date of ECG
Description

Date

Data type

date

Alias
UMLS CUI [1]
C0011008
Any pathologic findings in ECG?
Description

ECG findings

Data type

boolean

Alias
UMLS CUI [1]
C0438154
Please specify any pathologic ECG findings
Description

ECG findings

Data type

text

Alias
UMLS CUI [1]
C0438154
Did any of the events listed below happen after randomization but before CABG surgery? If yes, please fill in the outcome event form.
Description

Outcome events

Data type

text

Alias
UMLS CUI [1,1]
C1547647
UMLS CUI [1,2]
C0441471
Did the patient take antiplatelet agents the day before surgery?
Description

Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Please choose from the list below, which antiplatelet drug the patient took
Description

Antiplatelet drugs

Data type

text

Alias
UMLS CUI [1]
C0085826
Please specify which antiplatelet drugs the patient took, if you chose "other" or "more than one"
Description

Antiplatelet drugs

Data type

text

Alias
UMLS CUI [1]
C0085826
Did the patient take any anticoagulants the day before surgery?
Description

Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Please choose which one of the anticoagulants listed below the patient took.
Description

Anticoagulants

Data type

integer

Alias
UMLS CUI [1]
C0003280
Please specify which anticoagulant the patient took, if you chose "other" or "more than one".
Description

Anticoagulants

Data type

text

Alias
UMLS CUI [1]
C0003280
Did the patient take any antihypertensive drugs the day before surgery?
Description

Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Please choose which one of the antihypertensive drugs listed below the patient took.
Description

Antihypertensive drugs

Data type

text

Alias
UMLS CUI [1]
C0003364
Please specify which antihypertensive agent the patient took, if you chose "other" or "more than one".
Description

antihypertensive agent

Data type

text

Alias
UMLS CUI [1]
C0003364
Did the patient take any lipid lowering agents the day before surgery?
Description

Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Please choose which one of the antilipemic agents listed below the patient took
Description

Antilipemic agent

Data type

text

Alias
UMLS CUI [1]
C0003367
Please specify which antilipemic agent the patient took, if you chose "other" or "more than one".
Description

antilipemic agent

Data type

text

Alias
UMLS CUI [1]
C0003367
Any other relevant concomitant medication the patient took the day before surgery?
Description

Concomitant Medication

Data type

boolean

Alias
UMLS CUI [1]
C2347852
Please specify what other concomitant medication the patient took
Description

Concomitant Medication

Data type

text

Alias
UMLS CUI [1]
C2347852
Date of completion of this form
Description

Date of completion

Data type

date

Alias
UMLS CUI [1]
C0011008
Signature by investigator
Description

Signature

Data type

text

Alias
UMLS CUI [1]
C1519316
Name of Investigator
Description

Name of Investigator

Data type

text

Alias
UMLS CUI [1]
C0008961
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Similar models

CABACS Case Report Form [Baseline visit]

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Baseline Examination
Date
Item
Date of visit
date
C0011008 (UMLS CUI [1])
Patient Study ID
Item
Patient ID
text
C2348585 (UMLS CUI [1])
ECG
Item
ECG done?
boolean
C1623258 (UMLS CUI [1])
Date
Item
Date of ECG
date
C0011008 (UMLS CUI [1])
ECG findings
Item
Any pathologic findings in ECG?
boolean
C0438154 (UMLS CUI [1])
ECG findings
Item
Please specify any pathologic ECG findings
text
C0438154 (UMLS CUI [1])
Item
Did any of the events listed below happen after randomization but before CABG surgery? If yes, please fill in the outcome event form.
text
C1547647 (UMLS CUI [1,1])
C0441471 (UMLS CUI [1,2])
Outcome events
Code List
Did any of the events listed below happen after randomization but before CABG surgery? If yes, please fill in the outcome event form.
CL Item
Stroke (1)
CL Item
Myocardial infarction (2)
CL Item
Death (3)
CL Item
Not applicable (4)
Concomitant Medication
Item
Did the patient take antiplatelet agents the day before surgery?
boolean
C2347852 (UMLS CUI [1])
Item
Please choose from the list below, which antiplatelet drug the patient took
text
C0085826 (UMLS CUI [1])
Antiplatelet drugs
Code List
Please choose from the list below, which antiplatelet drug the patient took
CL Item
Acetyl salicylic acid (1)
CL Item
Clopidogrel (2)
CL Item
Acetyl salicylic acid plus Dipyridamole (3)
CL Item
More than one of the list (4)
CL Item
Other (5)
Antiplatelet drugs
Item
Please specify which antiplatelet drugs the patient took, if you chose "other" or "more than one"
text
C0085826 (UMLS CUI [1])
Concomitant Medication
Item
Did the patient take any anticoagulants the day before surgery?
boolean
C2347852 (UMLS CUI [1])
Item
Please choose which one of the anticoagulants listed below the patient took.
integer
C0003280 (UMLS CUI [1])
Anticoagulant type
Code List
Please choose which one of the anticoagulants listed below the patient took.
CL Item
Unfractionated heparin IV (1)
CL Item
Full dose LMW heparin (Enoxaparin , Others) (2)
CL Item
Vitamin K Antagonists like Warfarin (Coumadin) (3)
CL Item
Dabigatran (4)
CL Item
Other (5)
CL Item
More than one of the list (6)
Anticoagulants
Item
Please specify which anticoagulant the patient took, if you chose "other" or "more than one".
text
C0003280 (UMLS CUI [1])
Concomitant Medication
Item
Did the patient take any antihypertensive drugs the day before surgery?
boolean
C2347852 (UMLS CUI [1])
Item
Please choose which one of the antihypertensive drugs listed below the patient took.
text
C0003364 (UMLS CUI [1])
Antihypertensive drugs
Code List
Please choose which one of the antihypertensive drugs listed below the patient took.
CL Item
ACE inhibitor (1)
CL Item
angiotensin receptor blocker (2)
CL Item
Diuretics (3)
CL Item
Calcium Antagonist (4)
CL Item
Beta blocker (5)
CL Item
Other (6)
CL Item
More than one of the list (7)
antihypertensive agent
Item
Please specify which antihypertensive agent the patient took, if you chose "other" or "more than one".
text
C0003364 (UMLS CUI [1])
Concomitant Medication
Item
Did the patient take any lipid lowering agents the day before surgery?
boolean
C2347852 (UMLS CUI [1])
Item
Please choose which one of the antilipemic agents listed below the patient took
text
C0003367 (UMLS CUI [1])
Antilipemic agent
Code List
Please choose which one of the antilipemic agents listed below the patient took
CL Item
Statine (1)
CL Item
Other (2)
CL Item
More than one (3)
antilipemic agent
Item
Please specify which antilipemic agent the patient took, if you chose "other" or "more than one".
text
C0003367 (UMLS CUI [1])
Concomitant Medication
Item
Any other relevant concomitant medication the patient took the day before surgery?
boolean
C2347852 (UMLS CUI [1])
Concomitant Medication
Item
Please specify what other concomitant medication the patient took
text
C2347852 (UMLS CUI [1])
Date of completion
Item
Date of completion of this form
date
C0011008 (UMLS CUI [1])
Signature
Item
Signature by investigator
text
C1519316 (UMLS CUI [1])
Name of Investigator
Item
Name of Investigator
text
C0008961 (UMLS CUI [1])
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