ID

13390

Description

Collection of Blood, Bone Marrow, Tumor, or Tissue Samples From Patients With Cancer to Study Drug Resistance; ODM derived from: https://clinicaltrials.gov/show/NCT00026663

Lien

https://clinicaltrials.gov/show/NCT00026663

Mots-clés

  1. 10/02/2016 10/02/2016 -
Téléchargé le

10 février 2016

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Renal Cell Carcinoma NCT00026663

Eligibility Renal Cell Carcinoma NCT00026663

Criteria
Description

Criteria

1. patients 18 years of age and older are eligible.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
2. patients must have a performance status of ecog 0, 1, 2, or 3 for admission to this protocol.
Description

ecog

Type de données

boolean

Alias
UMLS CUI [1]
C1520224
3. patients with malignancy are eligible.
Description

malignancy

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
4. patients requiring a surgical procedure for any medical indication can be included on study.
Description

surgery

Type de données

boolean

Alias
UMLS CUI [1]
C0543467
5. patients requiring biopsy or any procedure for any medical indication can be included on study.
Description

biopsy, medical procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0005558
UMLS CUI [2]
C0199171
6. patients not requiring biopsy for a medical indication can be included on the study solely for the purpose of obtaining research samples, including blood, pleural fluid, or peritoneal fluid, or biopsy samples, providing the biopsy or aspiration procedure is of minimal risk, i.e. fine needle aspirate, bone marrow aspirate, or excisional biopsy. no radiology tests will be used in the procedure to collect a sample that would not be otherwise used for an appropriate medical indication.
Description

research

Type de données

boolean

Alias
UMLS CUI [1]
C0035168
7. normal volunteers 18 years of age and older are eligible to enroll. normal volunteers must be willing to sign informed consent and must be willing to provide samples to be used for research.
Description

informed consent

Type de données

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. pregnant individuals will not be eligible due to potential risks to the fetus associated with radiologic procedures required for biopsy.
Description

pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
2. children will not be eligible because of potential risks from complications due to procedures involved in obtaining the biopsies.
Description

age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
3. normal volunteers with a history of a clotting disorder may not enroll.
Description

clotting disorder

Type de données

boolean

Alias
UMLS CUI [1]
C0005779

Similar models

Eligibility Renal Cell Carcinoma NCT00026663

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
age
Item
1. patients 18 years of age and older are eligible.
boolean
C0001779 (UMLS CUI [1])
ecog
Item
2. patients must have a performance status of ecog 0, 1, 2, or 3 for admission to this protocol.
boolean
C1520224 (UMLS CUI [1])
malignancy
Item
3. patients with malignancy are eligible.
boolean
C0006826 (UMLS CUI [1])
surgery
Item
4. patients requiring a surgical procedure for any medical indication can be included on study.
boolean
C0543467 (UMLS CUI [1])
biopsy, medical procedure
Item
5. patients requiring biopsy or any procedure for any medical indication can be included on study.
boolean
C0005558 (UMLS CUI [1])
C0199171 (UMLS CUI [2])
research
Item
6. patients not requiring biopsy for a medical indication can be included on the study solely for the purpose of obtaining research samples, including blood, pleural fluid, or peritoneal fluid, or biopsy samples, providing the biopsy or aspiration procedure is of minimal risk, i.e. fine needle aspirate, bone marrow aspirate, or excisional biopsy. no radiology tests will be used in the procedure to collect a sample that would not be otherwise used for an appropriate medical indication.
boolean
C0035168 (UMLS CUI [1])
informed consent
Item
7. normal volunteers 18 years of age and older are eligible to enroll. normal volunteers must be willing to sign informed consent and must be willing to provide samples to be used for research.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy
Item
1. pregnant individuals will not be eligible due to potential risks to the fetus associated with radiologic procedures required for biopsy.
boolean
C0032961 (UMLS CUI [1])
age
Item
2. children will not be eligible because of potential risks from complications due to procedures involved in obtaining the biopsies.
boolean
C0001779 (UMLS CUI [1])
clotting disorder
Item
3. normal volunteers with a history of a clotting disorder may not enroll.
boolean
C0005779 (UMLS CUI [1])

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