ID

13232

Description

Trial of Daily Pulse Interleukin-2 With Famotidine in Acute Myelogenous Leukemia; ODM derived from: https://clinicaltrials.gov/show/NCT01289678

Lien

https://clinicaltrials.gov/show/NCT01289678

Mots-clés

  1. 25/01/2016 25/01/2016 -
Détendeur de droits

CC BY-NC 3.0

Téléchargé le

25 janvier 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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.

Groupe Item commentaires pour :

Item commentaires pour :

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

Eligibility Acute Myelogenous Leukemia NCT01289678

Eligibility Acute Myelogenous Leukemia NCT01289678

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
confirmed hematopathology diagnosis of aml receiving marrow suppressive treatment
Description

AML

Type de données

boolean

Alias
UMLS CUI [1]
C0023467
total wbc recovery of 500 mm3 prior to il-2 treatment
Description

Leukocytes

Type de données

boolean

Alias
UMLS CUI [1]
C0023508
platelet count of at least 20,000 mm3 prior to starting il-2 treatment
Description

platelets

Type de données

boolean

Alias
UMLS CUI [1]
C0005821
active infection controlled prior to starting il-2 treatment
Description

infection

Type de données

boolean

Alias
UMLS CUI [1]
C0009450
stable systolic blood pressure > 90mm hg prior to starting il-2 treatment
Description

blood pressure

Type de données

boolean

Alias
UMLS CUI [1]
C0005823
o2 saturation >90% prior to starting treatment
Description

oxygen saturation

Type de données

boolean

Alias
UMLS CUI [1]
C0523807
stable cardiopulmonary status prior to starting il-2 treatment
Description

health status

Type de données

boolean

Alias
UMLS CUI [1]
C0018759
serum creatinine < or equal to 2.0 mg/dl
Description

creatinine

Type de données

boolean

Alias
UMLS CUI [1]
C0201976
total bilirubin and ast <3x upper limits normal
Description

bilirubin

Type de données

boolean

Alias
UMLS CUI [1]
C1278039
UMLS CUI [2]
C0201899
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute promyelocytic leukemia
Description

APL

Type de données

boolean

Alias
UMLS CUI [1]
C0023487
active thrombocytopenic bleeding
Description

thrombocytopenia

Type de données

boolean

Alias
UMLS CUI [1]
C0040034
cardiac ejection fraction below 45%
Description

cardiac ejection fraction

Type de données

boolean

Alias
UMLS CUI [1]
C0232174
pregnancy and/or lactation
Description

pregnancy and/or lactation

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147

Similar models

Eligibility Acute Myelogenous Leukemia NCT01289678

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
AML
Item
confirmed hematopathology diagnosis of aml receiving marrow suppressive treatment
boolean
C0023467 (UMLS CUI [1])
Leukocytes
Item
total wbc recovery of 500 mm3 prior to il-2 treatment
boolean
C0023508 (UMLS CUI [1])
platelets
Item
platelet count of at least 20,000 mm3 prior to starting il-2 treatment
boolean
C0005821 (UMLS CUI [1])
infection
Item
active infection controlled prior to starting il-2 treatment
boolean
C0009450 (UMLS CUI [1])
blood pressure
Item
stable systolic blood pressure > 90mm hg prior to starting il-2 treatment
boolean
C0005823 (UMLS CUI [1])
oxygen saturation
Item
o2 saturation >90% prior to starting treatment
boolean
C0523807 (UMLS CUI [1])
health status
Item
stable cardiopulmonary status prior to starting il-2 treatment
boolean
C0018759 (UMLS CUI [1])
creatinine
Item
serum creatinine < or equal to 2.0 mg/dl
boolean
C0201976 (UMLS CUI [1])
bilirubin
Item
total bilirubin and ast <3x upper limits normal
boolean
C1278039 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
APL
Item
acute promyelocytic leukemia
boolean
C0023487 (UMLS CUI [1])
thrombocytopenia
Item
active thrombocytopenic bleeding
boolean
C0040034 (UMLS CUI [1])
cardiac ejection fraction
Item
cardiac ejection fraction below 45%
boolean
C0232174 (UMLS CUI [1])
pregnancy and/or lactation
Item
pregnancy and/or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])

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

Les champs marqués d’un * sont obligatoires.

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