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ID

15781

Beschrijving

Safety and Efficacy of FolateScan (Technetium Tc 99m EC20) in Subjects With Suspected Metastatic Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT01689662

Link

https://clinicaltrials.gov/show/NCT01689662

Trefwoorden

  1. 13-06-16 13-06-16 -
Geüploaded op

13 juni 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Metastatic Renal Cell Carcinoma NCT01689662

Eligibility Metastatic Renal Cell Carcinoma NCT01689662

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. subject must be 18 years of age or older.
Beschrijving

subjects must meet the following eligibility requirements to be enrolled in the study.

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
2. subject must have known or strongly suspected metastatic renal cell carcinoma with at least one target lesion as identified by ultrasonography, mri, or ct.
Beschrijving

metastatic renal cell carcinoma

Datatype

boolean

Alias
UMLS CUI [1]
C0278678
3. subject must have good kidney function.
Beschrijving

kidney function

Datatype

boolean

Alias
UMLS CUI [1]
C0232804
4. subject must provide written informed consent prior to enrollment.
Beschrijving

written informed

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. subject is pregnant or breastfeeding.
Beschrijving

subjects must be excluded if any of the following conditions are present:

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
2. subject is simultaneously participating in another investigational drug study, excluding the follow-up phase.
Beschrijving

participating in another study

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
3. subject has received an investigational agent within 7 days prior to enrollment.
Beschrijving

investigational agent

Datatype

boolean

Alias
UMLS CUI [1]
C1875319
4. subject is unable to tolerate conditions for radionuclide imaging.
Beschrijving

radionuclide imaging

Datatype

boolean

Alias
UMLS CUI [1]
C0034606
5. subject has been administered another radiopharmaceutical that would interfere with the assessment of technetium tc 99m ec20.
Beschrijving

technetium tc 99m ec20

Datatype

boolean

Alias
UMLS CUI [1,1]
C0182638
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C1883272

Similar models

Eligibility Metastatic Renal Cell Carcinoma NCT01689662

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
1. subject must be 18 years of age or older.
boolean
C0001779 (UMLS CUI [1])
metastatic renal cell carcinoma
Item
2. subject must have known or strongly suspected metastatic renal cell carcinoma with at least one target lesion as identified by ultrasonography, mri, or ct.
boolean
C0278678 (UMLS CUI [1])
kidney function
Item
3. subject must have good kidney function.
boolean
C0232804 (UMLS CUI [1])
written informed
Item
4. subject must provide written informed consent prior to enrollment.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
pregnancy or breast-feeding
Item
1. subject is pregnant or breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
participating in another study
Item
2. subject is simultaneously participating in another investigational drug study, excluding the follow-up phase.
boolean
C2348568 (UMLS CUI [1])
investigational agent
Item
3. subject has received an investigational agent within 7 days prior to enrollment.
boolean
C1875319 (UMLS CUI [1])
radionuclide imaging
Item
4. subject is unable to tolerate conditions for radionuclide imaging.
boolean
C0034606 (UMLS CUI [1])
technetium tc 99m ec20
Item
5. subject has been administered another radiopharmaceutical that would interfere with the assessment of technetium tc 99m ec20.
boolean
C0182638 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C1883272 (UMLS CUI [1,3])

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