ID

28366

Beschrijving

Figitumumab Combined With Pegvisomant For Advanced Solid Tumors; ODM derived from: https://clinicaltrials.gov/show/NCT00976508

Link

https://clinicaltrials.gov/show/NCT00976508

Trefwoorden

  1. 08-01-18 08-01-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

8 januari 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Colorectal Neoplasms NCT00976508

Eligibility Colorectal Neoplasms NCT00976508

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients ≥18 years of age with advanced solid tumors for which the combination of figitumumab and pegvisomant are reasonable treatment options.
Beschrijving

Age | Solid tumour Advanced | Treatment options Combined Modality Therapy | figitumumab | pegvisomant

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0280100
UMLS CUI [2,2]
C0205179
UMLS CUI [3,1]
C0683525
UMLS CUI [3,2]
C0009429
UMLS CUI [4]
C2713009
UMLS CUI [5]
C0913469
patients between the ages of 10 and 18 years with advanced sarcomas for which there is no available curative therapy or therapy proven to prolong survival with an acceptable quality of life will be included in the sarcoma expansion cohort.
Beschrijving

Age | Sarcoma Advanced | Curative treatment Lacking | Therapeutic procedure Proven Lacking | Survival Problem | Quality of life Problem

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C1261473
UMLS CUI [2,2]
C0205179
UMLS CUI [3,1]
C1273390
UMLS CUI [3,2]
C0332268
UMLS CUI [4,1]
C0087111
UMLS CUI [4,2]
C0456369
UMLS CUI [4,3]
C0332268
UMLS CUI [5,1]
C0038952
UMLS CUI [5,2]
C0033213
UMLS CUI [6,1]
C0034380
UMLS CUI [6,2]
C0033213
adequate recovery from prior therapies.
Beschrijving

Prior Therapy | Patient recovered

Datatype

boolean

Alias
UMLS CUI [1]
C1514463
UMLS CUI [2]
C1115804
adequate organ function (i.e. bone marrow, kidney, liver)
Beschrijving

Organ function | Bone Marrow function | Renal function | Liver function

Datatype

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2,1]
C0005953
UMLS CUI [2,2]
C0031843
UMLS CUI [3]
C0232804
UMLS CUI [4]
C0232741
total igf-1 ≥100 ng/ml (13 nmol/l).
Beschrijving

Insulin-Like Growth Factor I

Datatype

boolean

Alias
UMLS CUI [1]
C0021665
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
concurrent treatment with any anti-tumor agents.
Beschrijving

Antineoplastic Agents

Datatype

boolean

Alias
UMLS CUI [1]
C0003392
pregnant or breastfeeding females.
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
significant past history or active cardiac disease
Beschrijving

Heart Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0018799
active infection
Beschrijving

Communicable Disease

Datatype

boolean

Alias
UMLS CUI [1]
C0009450
history of diabetes mellitus.
Beschrijving

Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
glycosylated hemoglobin >5.7
Beschrijving

Glycosylated hemoglobin measurement

Datatype

boolean

Alias
UMLS CUI [1]
C0202054

Similar models

Eligibility Colorectal Neoplasms NCT00976508

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Solid tumour Advanced | Treatment options Combined Modality Therapy | figitumumab | pegvisomant
Item
patients ≥18 years of age with advanced solid tumors for which the combination of figitumumab and pegvisomant are reasonable treatment options.
boolean
C0001779 (UMLS CUI [1])
C0280100 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C0683525 (UMLS CUI [3,1])
C0009429 (UMLS CUI [3,2])
C2713009 (UMLS CUI [4])
C0913469 (UMLS CUI [5])
Age | Sarcoma Advanced | Curative treatment Lacking | Therapeutic procedure Proven Lacking | Survival Problem | Quality of life Problem
Item
patients between the ages of 10 and 18 years with advanced sarcomas for which there is no available curative therapy or therapy proven to prolong survival with an acceptable quality of life will be included in the sarcoma expansion cohort.
boolean
C0001779 (UMLS CUI [1])
C1261473 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C1273390 (UMLS CUI [3,1])
C0332268 (UMLS CUI [3,2])
C0087111 (UMLS CUI [4,1])
C0456369 (UMLS CUI [4,2])
C0332268 (UMLS CUI [4,3])
C0038952 (UMLS CUI [5,1])
C0033213 (UMLS CUI [5,2])
C0034380 (UMLS CUI [6,1])
C0033213 (UMLS CUI [6,2])
Prior Therapy | Patient recovered
Item
adequate recovery from prior therapies.
boolean
C1514463 (UMLS CUI [1])
C1115804 (UMLS CUI [2])
Organ function | Bone Marrow function | Renal function | Liver function
Item
adequate organ function (i.e. bone marrow, kidney, liver)
boolean
C0678852 (UMLS CUI [1])
C0005953 (UMLS CUI [2,1])
C0031843 (UMLS CUI [2,2])
C0232804 (UMLS CUI [3])
C0232741 (UMLS CUI [4])
Insulin-Like Growth Factor I
Item
total igf-1 ≥100 ng/ml (13 nmol/l).
boolean
C0021665 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Antineoplastic Agents
Item
concurrent treatment with any anti-tumor agents.
boolean
C0003392 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding females.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Heart Disease
Item
significant past history or active cardiac disease
boolean
C0018799 (UMLS CUI [1])
Communicable Disease
Item
active infection
boolean
C0009450 (UMLS CUI [1])
Diabetes Mellitus
Item
history of diabetes mellitus.
boolean
C0011849 (UMLS CUI [1])
Glycosylated hemoglobin measurement
Item
glycosylated hemoglobin >5.7
boolean
C0202054 (UMLS CUI [1])

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