ID

12771

Beschrijving

Same Day Versus Next Day Discharge: Ambulatory Closure Device Percutaneous Intervention; ODM derived from: https://clinicaltrials.gov/show/NCT01230606

Link

https://clinicaltrials.gov/show/NCT01230606

Trefwoorden

Versies (1)
  1. 21-12-15 21-12-15 -
Geüploaded op

21 december 2015

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Cardiovascular Disease NCT01230606

Engels

Eligibility Cardiovascular Disease NCT01230606

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. <75 years of age at the time of procedure.
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
2. patient has a type a or b lesion(s)
Beschrijving

lesion

Datatype

boolean

Alias
UMLS CUI [1]
C0221198
3. femoral access site is amenable to closure with a vascular closure device.
Beschrijving

vascular closure device

Datatype

boolean

Alias
UMLS CUI [1]
C3504161
4. over 2 hours since the completion of the pci procedure (at least 2 hours must elapse from completion of the pci before subjects become eligible).
Beschrijving

Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C1532338
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patient has a life expectancy less than 12 months.
Beschrijving

life expectancy

Datatype

boolean

Alias
UMLS CUI [1]
C0023671
2. patient has recent evidence of an acute coronary syndrome (mi)
Beschrijving

acute coronary syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0948089
3. femoral access is difficult or site is not amenable to closure device
Beschrijving

access femoral

Datatype

boolean

Alias
UMLS CUI [1,1]
C0444454
UMLS CUI [1,2]
C0015811
4. anticoagulants other than unfractionated heparin or bivalirudin were used during the procedure (i.e. enoxaparin).
Beschrijving

anticoagulants

Datatype

boolean

Alias
UMLS CUI [1]
C0003280
5. patient has sub optimal angiographic outcome or clinical complication(s) during pci
Beschrijving

Percutaneous Coronary Intervention; angiogram

Datatype

boolean

Alias
UMLS CUI [1]
C1532338
UMLS CUI [2]
C0002978
6. the pci occurred in something other than a native coronary artery
Beschrijving

Percutaneous Coronary Intervention; Coronary artery

Datatype

boolean

Alias
UMLS CUI [1]
C1532338
UMLS CUI [2]
C0205042
7. angiographic evidence of thrombus
Beschrijving

thrombus; angiogram

Datatype

boolean

Alias
UMLS CUI [1]
C0087086
UMLS CUI [2]
C0002978
8. patient has more than 3 stents implanted during this pci
Beschrijving

stent; Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C0038257
UMLS CUI [2]
C1532338
9. patient has an inr >2, platelet count <100,000 or hematocrit <25
Beschrijving

International Normalized Ratio; Platelet Count measurement; Platelet hematocrit measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0525032
UMLS CUI [2]
C0032181
UMLS CUI [3]
C0474566
10. occlusion of major side branch during pci of >1.5mm
Beschrijving

occlusion; Percutaneous Coronary Intervention

Datatype

boolean

Alias
UMLS CUI [1]
C1947917
UMLS CUI [2]
C1532338
11. patient has ejection fraction ≤30%
Beschrijving

ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0232174
12. known allergy to pci procedural medications
Beschrijving

hypersensitivity Percutaneous Coronary Intervention medication

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1532338
UMLS CUI [1,3]
C0013227
13. patient reports living further than 30 minutes from a hospital by ambulance.
Beschrijving

residence patient

Datatype

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0030705
14. patient provides informed consent and agrees to the follow-up schedule.
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
15. evidence of vascular complication(s) (e.g. dissection, hematoma, bleeding) peri-procedure
Beschrijving

vascular complication

Datatype

boolean

Alias
UMLS CUI [1]
C1112391
16. patient is pregnant
Beschrijving

pregnant

Datatype

boolean

Alias
UMLS CUI [1]
C0549206
17. evidence of infection (e.g. fever, pus, swelling) peri-procedure
Beschrijving

infection

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
18. patients with chronic renal insufficiency (e.g. serum creatinine ≥1.5 mg/dl)
Beschrijving

chronic renal insufficiency

Datatype

boolean

Alias
UMLS CUI [1]
C0022661
Terug naar het begin van de pagina

Similar models

Eligibility Cardiovascular Disease NCT01230606

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
1. <75 years of age at the time of procedure.
boolean
C0001779 (UMLS CUI [1])
lesion
Item
2. patient has a type a or b lesion(s)
boolean
C0221198 (UMLS CUI [1])
vascular closure device
Item
3. femoral access site is amenable to closure with a vascular closure device.
boolean
C3504161 (UMLS CUI [1])
Percutaneous Coronary Intervention
Item
4. over 2 hours since the completion of the pci procedure (at least 2 hours must elapse from completion of the pci before subjects become eligible).
boolean
C1532338 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
life expectancy
Item
1. patient has a life expectancy less than 12 months.
boolean
C0023671 (UMLS CUI [1])
acute coronary syndrome
Item
2. patient has recent evidence of an acute coronary syndrome (mi)
boolean
C0948089 (UMLS CUI [1])
access femoral
Item
3. femoral access is difficult or site is not amenable to closure device
boolean
C0444454 (UMLS CUI [1,1])
C0015811 (UMLS CUI [1,2])
anticoagulants
Item
4. anticoagulants other than unfractionated heparin or bivalirudin were used during the procedure (i.e. enoxaparin).
boolean
C0003280 (UMLS CUI [1])
Percutaneous Coronary Intervention; angiogram
Item
5. patient has sub optimal angiographic outcome or clinical complication(s) during pci
boolean
C1532338 (UMLS CUI [1])
C0002978 (UMLS CUI [2])
Percutaneous Coronary Intervention; Coronary artery
Item
6. the pci occurred in something other than a native coronary artery
boolean
C1532338 (UMLS CUI [1])
C0205042 (UMLS CUI [2])
thrombus; angiogram
Item
7. angiographic evidence of thrombus
boolean
C0087086 (UMLS CUI [1])
C0002978 (UMLS CUI [2])
stent; Percutaneous Coronary Intervention
Item
8. patient has more than 3 stents implanted during this pci
boolean
C0038257 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
International Normalized Ratio; Platelet Count measurement; Platelet hematocrit measurement
Item
9. patient has an inr >2, platelet count <100,000 or hematocrit <25
boolean
C0525032 (UMLS CUI [1])
C0032181 (UMLS CUI [2])
C0474566 (UMLS CUI [3])
occlusion; Percutaneous Coronary Intervention
Item
10. occlusion of major side branch during pci of >1.5mm
boolean
C1947917 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
ejection fraction
Item
11. patient has ejection fraction ≤30%
boolean
C0232174 (UMLS CUI [1])
hypersensitivity Percutaneous Coronary Intervention medication
Item
12. known allergy to pci procedural medications
boolean
C0020517 (UMLS CUI [1,1])
C1532338 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
residence patient
Item
13. patient reports living further than 30 minutes from a hospital by ambulance.
boolean
C0237096 (UMLS CUI [1,1])
C0030705 (UMLS CUI [1,2])
informed consent
Item
14. patient provides informed consent and agrees to the follow-up schedule.
boolean
C0021430 (UMLS CUI [1])
vascular complication
Item
15. evidence of vascular complication(s) (e.g. dissection, hematoma, bleeding) peri-procedure
boolean
C1112391 (UMLS CUI [1])
pregnant
Item
16. patient is pregnant
boolean
C0549206 (UMLS CUI [1])
infection
Item
17. evidence of infection (e.g. fever, pus, swelling) peri-procedure
boolean
C0009450 (UMLS CUI [1])
chronic renal insufficiency
Item
18. patients with chronic renal insufficiency (e.g. serum creatinine ≥1.5 mg/dl)
boolean
C0022661 (UMLS CUI [1])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial