ID

20421

Description

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

Lien

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

Mots-clés

Versions (1)
  1. 22/02/2017 22/02/2017 -
Téléchargé le

22 février 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

  • Plus récent
  • Plus ancien
  • Favori
  • Plus récent
    • Plus récent
    • Plus ancien
    • Favori

Aucun commentaire

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

Anglais

Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulaires  
Trial Completion
Description

Trial Completion

Alias
UMLS CUI-1
C2732579
1. The patient completed planned observation time according to protocol
Description

patient completed planned observation time

Type de données

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0040223
2. If no please specify why:
Description

if no

Type de données

integer

Alias
UMLS CUI [1]
C2348235
Explain:
Description

Explanation

Type de données

text

Alias
UMLS CUI [1]
C0681841
Invenstigator´s Declaration
Description

Invenstigator´s Declaration

Alias
UMLS CUI-1
C0008961
3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
Description

Invenstigator´s Declaration

Type de données

text

Alias
UMLS CUI [1,1]
C0008961
UMLS CUI [1,2]
C1442085
Investigator´s signature
Description

Investigator´s signature

Type de données

text

Alias
UMLS CUI [1]
C2346576
Date of Signature
Description

Date of Signature

Type de données

date

Alias
UMLS CUI [1,1]
C0011008
UMLS CUI [1,2]
C1519316
Retour au début de la page

Similar models

Trial Completion PRoFESS - Prevention Regimen For Effectively Avoiding Second Strokes NCT00153062

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Trial Completion
C2732579 (UMLS CUI-1)
patient completed planned observation time
Item
1. The patient completed planned observation time according to protocol
boolean
C0525058 (UMLS CUI [1,1])
C0040223 (UMLS CUI [1,2])
Item
2. If no please specify why:
integer
C2348235 (UMLS CUI [1])
if no
Code List
2. If no please specify why:
CL Item
Death (must me recorded on death form) (1)
CL Item
Adverse Event (explain below) (2)
CL Item
Non compliant with protocol (explain below) (3)
CL Item
Lost follow-up (explain below) (4)
CL Item
Consent withdrawn (not due to adverse event, explain below) (5)
CL Item
Other (explain below) (6)
Explanation
Item
Explain:
text
C0681841 (UMLS CUI [1])
Item Group
Invenstigator´s Declaration
C0008961 (UMLS CUI-1)
Invenstigator´s Declaration
Item
3. Invenstigator´s Declaration By signing and dating this page, I declare that I have reviewed for accuracy all case report form pages for this patient; the information contained on these pages accurately reflects the medical record including the results of tests and evaluations performed in the dates specified.
text
C0008961 (UMLS CUI [1,1])
C1442085 (UMLS CUI [1,2])
Investigator´s signature
Item
Investigator´s signature
text
C2346576 (UMLS CUI [1])
Date of Signature
Item
Date of Signature
date
C0011008 (UMLS CUI [1,1])
C1519316 (UMLS CUI [1,2])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

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