ID

35170

Description

Intraoperative Dual-modality Imaging in Renal Cell Carcinoma; ODM derived from: https://clinicaltrials.gov/show/NCT02497599

Link

https://clinicaltrials.gov/show/NCT02497599

Keywords

  1. 2/20/19 2/20/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

February 20, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Carcinoma, Renal Cell NCT02497599

Eligibility Carcinoma, Renal Cell NCT02497599

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
clinical diagnosis of clear cell renal cell carcinoma planned for surgery, (partial) nephrectomy
Description

Clear Cell Renal Cell Carcinoma | Operative Surgical Procedures Planned | Nephrectomy Planned | Partial nephrectomy Planned

Data type

boolean

Alias
UMLS CUI [1]
C0279702
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C1301732
UMLS CUI [3,1]
C0027695
UMLS CUI [3,2]
C1301732
UMLS CUI [4,1]
C0194086
UMLS CUI [4,2]
C1301732
performance status: karnofsky 70 %
Description

Karnofsky Performance Status

Data type

boolean

Alias
UMLS CUI [1]
C0206065
being fit for surgery
Description

Fit Operative Surgical Procedures

Data type

boolean

Alias
UMLS CUI [1,1]
C0424576
UMLS CUI [1,2]
C0543467
minimum age 18 years
Description

Age Minimum

Data type

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1524031
signed informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
a known subtype other than clear cell rcc
Description

Subtype Except Clear Cell Renal Cell Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C0449560
UMLS CUI [1,2]
C0332300
UMLS CUI [1,3]
C0279702
any medical condition present that in the opinion of the investigator will affect patients' clinical status.
Description

Medical condition Affecting Patient Clinical status

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0030705
UMLS CUI [1,4]
C0449440
administration of a radioisotope within 10 physical half lives prior to study enrollment
Description

Administration Radioisotope

Data type

boolean

Alias
UMLS CUI [1,1]
C1533734
UMLS CUI [1,2]
C0034595
pregnancy and lactation
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
evidence of qt prolongation on screening ecg
Description

Prolonged QT interval ECG

Data type

boolean

Alias
UMLS CUI [1,1]
C0151878
UMLS CUI [1,2]
C0013798
had within 6 months prior to enrollment: myocardial infarction, uncontrolled heart failure, or unstable angina pectoris.
Description

Myocardial Infarction | Heart failure Uncontrolled | Angina, Unstable

Data type

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2,1]
C0018801
UMLS CUI [2,2]
C0205318
UMLS CUI [3]
C0002965

Similar models

Eligibility Carcinoma, Renal Cell NCT02497599

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Clear Cell Renal Cell Carcinoma | Operative Surgical Procedures Planned | Nephrectomy Planned | Partial nephrectomy Planned
Item
clinical diagnosis of clear cell renal cell carcinoma planned for surgery, (partial) nephrectomy
boolean
C0279702 (UMLS CUI [1])
C0543467 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0027695 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0194086 (UMLS CUI [4,1])
C1301732 (UMLS CUI [4,2])
Karnofsky Performance Status
Item
performance status: karnofsky 70 %
boolean
C0206065 (UMLS CUI [1])
Fit Operative Surgical Procedures
Item
being fit for surgery
boolean
C0424576 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
Age Minimum
Item
minimum age 18 years
boolean
C0001779 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Subtype Except Clear Cell Renal Cell Carcinoma
Item
a known subtype other than clear cell rcc
boolean
C0449560 (UMLS CUI [1,1])
C0332300 (UMLS CUI [1,2])
C0279702 (UMLS CUI [1,3])
Medical condition Affecting Patient Clinical status
Item
any medical condition present that in the opinion of the investigator will affect patients' clinical status.
boolean
C3843040 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0030705 (UMLS CUI [1,3])
C0449440 (UMLS CUI [1,4])
Administration Radioisotope
Item
administration of a radioisotope within 10 physical half lives prior to study enrollment
boolean
C1533734 (UMLS CUI [1,1])
C0034595 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnancy and lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Prolonged QT interval ECG
Item
evidence of qt prolongation on screening ecg
boolean
C0151878 (UMLS CUI [1,1])
C0013798 (UMLS CUI [1,2])
Myocardial Infarction | Heart failure Uncontrolled | Angina, Unstable
Item
had within 6 months prior to enrollment: myocardial infarction, uncontrolled heart failure, or unstable angina pectoris.
boolean
C0027051 (UMLS CUI [1])
C0018801 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0002965 (UMLS CUI [3])

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