ID

37572

Descrição

the Study of STABLE_SR for Persistent Atrial Fibrillation; ODM derived from: https://clinicaltrials.gov/show/NCT01761188

Link

https://clinicaltrials.gov/show/NCT01761188

Palavras-chave

  1. 08/08/2019 08/08/2019 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

8 de agosto de 2019

DOI

Para um pedido faça login.

Licença

Creative Commons BY 4.0

Comentários do modelo :

Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.

Comentários do grupo de itens para :

Comentários do item para :

Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.

Eligibility Atrial Fibrillation NCT01761188

Eligibility Atrial Fibrillation NCT01761188

Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing a first-time ablation procedure for af;
Descrição

Catheter ablation for atrial fibrillation Firstly

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2702800
UMLS CUI [1,2]
C1279901
patients with persistent or long-lasting af; persistent af will be defined as a sustained episode lasting > 7 days and less than 1 years; long-lasting persistent af will be more than 1 year and less than 5 years.
Descrição

Persistent atrial fibrillation Episode Duration | Longstanding persistent atrial fibrillation Duration

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C2585653
UMLS CUI [1,2]
C0332189
UMLS CUI [1,3]
C0449238
UMLS CUI [2,1]
C3873617
UMLS CUI [2,2]
C0449238
patients must be willing and able to comply with all peri-ablation and follow-up requirements.
Descrição

Protocol Compliance

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0525058
patients with atrial fibrillation will to accept the procedure of ablation.
Descrição

Atrial Fibrillation | Agreement Ablation

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0004238
UMLS CUI [2,1]
C0680240
UMLS CUI [2,2]
C0547070
patients signed the written informed consent for the study.
Descrição

Informed Consent

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
patients can endure the required follow up.
Descrição

Compliance Follow-up

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C3274571
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with paroxysmal af; paroxysmal af will be defined as a sustained episode lasting < 7days.
Descrição

Paroxysmal atrial fibrillation Episode Duration

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0235480
UMLS CUI [1,2]
C0332189
UMLS CUI [1,3]
C0449238
patients with contraindications to systemic anticoagulation with heparin or coumadin or a direct thrombin inhibitor.
Descrição

Medical contraindication Anticoagulation Therapy Systemic | Medical contraindication Heparin | Medical contraindication Coumadin | Medical contraindication Direct Thrombin Inhibitor

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0003281
UMLS CUI [1,3]
C0205373
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C0019134
UMLS CUI [3,1]
C1301624
UMLS CUI [3,2]
C0699129
UMLS CUI [4,1]
C1301624
UMLS CUI [4,2]
C3536847
patients with thromboemboli in laa.
Descrição

Thromboembolus Left Atrial Appendage

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0040038
UMLS CUI [1,2]
C4284918
patients with left atrial size ≥ 55 mm (2d echocardiography, parasternal long-axis view).
Descrição

Left atrium Size 2D Echocardiography Parasternal long axis view

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0225860
UMLS CUI [1,2]
C0456389
UMLS CUI [1,3]
C0013524
UMLS CUI [1,4]
C1302222
patients allergic for contrast or iodine.
Descrição

Contrast media allergy | Iodine allergy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0570562
UMLS CUI [2]
C0571818
patients with the scr >3.5mg/dl or ccr < 30 ml/min
Descrição

Creatinine measurement, serum | Creatinine clearance measurement

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C0373595
patients with life expectancy < 12 months
Descrição

Life Expectancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023671
patients who are in the period of pregnant
Descrição

Pregnancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961

Similar models

Eligibility Atrial Fibrillation NCT01761188

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Catheter ablation for atrial fibrillation Firstly
Item
patients undergoing a first-time ablation procedure for af;
boolean
C2702800 (UMLS CUI [1,1])
C1279901 (UMLS CUI [1,2])
Persistent atrial fibrillation Episode Duration | Longstanding persistent atrial fibrillation Duration
Item
patients with persistent or long-lasting af; persistent af will be defined as a sustained episode lasting > 7 days and less than 1 years; long-lasting persistent af will be more than 1 year and less than 5 years.
boolean
C2585653 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
C3873617 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Protocol Compliance
Item
patients must be willing and able to comply with all peri-ablation and follow-up requirements.
boolean
C0525058 (UMLS CUI [1])
Atrial Fibrillation | Agreement Ablation
Item
patients with atrial fibrillation will to accept the procedure of ablation.
boolean
C0004238 (UMLS CUI [1])
C0680240 (UMLS CUI [2,1])
C0547070 (UMLS CUI [2,2])
Informed Consent
Item
patients signed the written informed consent for the study.
boolean
C0021430 (UMLS CUI [1])
Compliance Follow-up
Item
patients can endure the required follow up.
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Paroxysmal atrial fibrillation Episode Duration
Item
patients with paroxysmal af; paroxysmal af will be defined as a sustained episode lasting < 7days.
boolean
C0235480 (UMLS CUI [1,1])
C0332189 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Medical contraindication Anticoagulation Therapy Systemic | Medical contraindication Heparin | Medical contraindication Coumadin | Medical contraindication Direct Thrombin Inhibitor
Item
patients with contraindications to systemic anticoagulation with heparin or coumadin or a direct thrombin inhibitor.
boolean
C1301624 (UMLS CUI [1,1])
C0003281 (UMLS CUI [1,2])
C0205373 (UMLS CUI [1,3])
C1301624 (UMLS CUI [2,1])
C0019134 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C0699129 (UMLS CUI [3,2])
C1301624 (UMLS CUI [4,1])
C3536847 (UMLS CUI [4,2])
Thromboembolus Left Atrial Appendage
Item
patients with thromboemboli in laa.
boolean
C0040038 (UMLS CUI [1,1])
C4284918 (UMLS CUI [1,2])
Left atrium Size 2D Echocardiography Parasternal long axis view
Item
patients with left atrial size ≥ 55 mm (2d echocardiography, parasternal long-axis view).
boolean
C0225860 (UMLS CUI [1,1])
C0456389 (UMLS CUI [1,2])
C0013524 (UMLS CUI [1,3])
C1302222 (UMLS CUI [1,4])
Contrast media allergy | Iodine allergy
Item
patients allergic for contrast or iodine.
boolean
C0570562 (UMLS CUI [1])
C0571818 (UMLS CUI [2])
Creatinine measurement, serum | Creatinine clearance measurement
Item
patients with the scr >3.5mg/dl or ccr < 30 ml/min
boolean
C0201976 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Life Expectancy
Item
patients with life expectancy < 12 months
boolean
C0023671 (UMLS CUI [1])
Pregnancy
Item
patients who are in the period of pregnant
boolean
C0032961 (UMLS CUI [1])

Use este formulário para feedback, perguntas e sugestões de aperfeiçoamento.

Campos marcados com * são obrigatórios.

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