ID

30762

Beskrivning

Dose Adaptation of Capecitabine Using Mobile Phone Toxicity Monitoring; ODM derived from: https://clinicaltrials.gov/show/NCT01053104

Länk

https://clinicaltrials.gov/show/NCT01053104

Nyckelord

  1. 2018-06-20 2018-06-20 -
Rättsinnehavare

See clinicaltrials.gov

Uppladdad den

20 juni 2018

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Metastatic Colorectal Cancer NCT01053104

Eligibility Metastatic Colorectal Cancer NCT01053104

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
metastatic colorectal or breast cancer patients commencing treatment on one of four specified regimens
Beskrivning

Colorectal cancer metastatic | Secondary malignant neoplasm of female breast | Start Therapeutic procedure

Datatyp

boolean

Alias
UMLS CUI [1]
C0948380
UMLS CUI [2]
C0346993
UMLS CUI [3,1]
C0439659
UMLS CUI [3,2]
C0087111
for metastatic colorectal cancer:
Beskrivning

Colorectal cancer metastatic

Datatyp

boolean

Alias
UMLS CUI [1]
C0948380
capecitabine 2000mg/m2 d 1-14, q 3 weekly and oxaliplatin 130mg/m2 d1 q 3 weekly (capox)
Beskrivning

Capecitabine Dosage | Oxaliplatin Dosage | CAPOX Regimen

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0671970
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0069717
UMLS CUI [2,2]
C0178602
UMLS CUI [3]
C1879915
capecitabine 2500mg/m2 d 1-14, q 3 weekly
Beskrivning

Capecitabine Dosage

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0671970
UMLS CUI [1,2]
C0178602
for metastatic breast cancer:
Beskrivning

Secondary malignant neoplasm of female breast

Datatyp

boolean

Alias
UMLS CUI [1]
C0346993
capecitabine 2000mg/m2d 1-14, q 3 weekly
Beskrivning

Capecitabine Dosage

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0671970
UMLS CUI [1,2]
C0178602
capecitabine 2000mg/m2 d 1-14, q 3 weekly and docetaxel 75mg/m2 d1 q 3 weekly
Beskrivning

Capecitabine Dosage | Docetaxel Dosage

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0671970
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0246415
UMLS CUI [2,2]
C0178602
age > 18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
fit to start at full (100%) starting dose of all drugs
Beskrivning

Fit Pharmaceutical Preparations Dose Full

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0424576
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C0443225
able and willing to use mobile phone
Beskrivning

Able to operate mobile phone | Use of Mobile Phone Willing

Datatyp

boolean

Alias
UMLS CUI [1]
C4274610
UMLS CUI [2,1]
C1524063
UMLS CUI [2,2]
C1136360
UMLS CUI [2,3]
C0600109
reasonable renal, liver and bone marrow function
Beskrivning

Renal function | Liver function | Bone Marrow function

Datatyp

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0232741
UMLS CUI [3,1]
C0005953
UMLS CUI [3,2]
C0031843
absolute neutrophil count (anc) >1.5 x 109/l
Beskrivning

Absolute neutrophil count

Datatyp

boolean

Alias
UMLS CUI [1]
C0948762
platelet count > 100 x 109/l
Beskrivning

Platelet Count measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0032181
total bilirubin <1.5 uln
Beskrivning

Serum total bilirubin measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C1278039
alt, ast < 2.5 x uln
Beskrivning

Alanine aminotransferase measurement | Aspartate aminotransferase measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0201836
UMLS CUI [2]
C0201899
alkaline phosphatase < 2.5 x uln
Beskrivning

Alkaline phosphatase measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0201850
no obvious contra indications to capecitabine or oxaliplatin or docetaxel
Beskrivning

Absence Medical contraindication Capecitabine | Absence Medical contraindication Oxaliplatin | Absence Medical contraindication Docetaxel

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0332197
UMLS CUI [1,2]
C1301624
UMLS CUI [1,3]
C0671970
UMLS CUI [2,1]
C0332197
UMLS CUI [2,2]
C1301624
UMLS CUI [2,3]
C0069717
UMLS CUI [3,1]
C0332197
UMLS CUI [3,2]
C1301624
UMLS CUI [3,3]
C0246415
patients must also be able to read, write and understand english.
Beskrivning

Able to read English Language | Able to write English Language | Comprehension English Language

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0584993
UMLS CUI [2,2]
C0376245
UMLS CUI [3,1]
C0233733
UMLS CUI [3,2]
C0376245
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who live in an area of no vodafone or orange mobile phone network - -
Beskrivning

Residence | Mobile Phone Network Lacking | Other Coding

Datatyp

boolean

Alias
UMLS CUI [1]
C0237096
UMLS CUI [2,1]
C1136360
UMLS CUI [2,2]
C1882071
UMLS CUI [2,3]
C0332268
UMLS CUI [3]
C3846158
patients participating in other cancer treatment trials
Beskrivning

Study Subject Participation Status | Cancer treatment

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0920425
moderate or severe renal impairment [creatinine clearance <30ml/min (calculated according to cockroft-gault formula)]
Beskrivning

Renal Insufficiency Moderate | Renal Insufficiency Severe | Estimation of creatinine clearance by Cockcroft-Gault formula

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205081
UMLS CUI [2,1]
C1565489
UMLS CUI [2,2]
C0205082
UMLS CUI [3]
C2711451

Similar models

Eligibility Metastatic Colorectal Cancer NCT01053104

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Colorectal cancer metastatic | Secondary malignant neoplasm of female breast | Start Therapeutic procedure
Item
metastatic colorectal or breast cancer patients commencing treatment on one of four specified regimens
boolean
C0948380 (UMLS CUI [1])
C0346993 (UMLS CUI [2])
C0439659 (UMLS CUI [3,1])
C0087111 (UMLS CUI [3,2])
Colorectal cancer metastatic
Item
for metastatic colorectal cancer:
boolean
C0948380 (UMLS CUI [1])
Capecitabine Dosage | Oxaliplatin Dosage | CAPOX Regimen
Item
capecitabine 2000mg/m2 d 1-14, q 3 weekly and oxaliplatin 130mg/m2 d1 q 3 weekly (capox)
boolean
C0671970 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0069717 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C1879915 (UMLS CUI [3])
Capecitabine Dosage
Item
capecitabine 2500mg/m2 d 1-14, q 3 weekly
boolean
C0671970 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Secondary malignant neoplasm of female breast
Item
for metastatic breast cancer:
boolean
C0346993 (UMLS CUI [1])
Capecitabine Dosage
Item
capecitabine 2000mg/m2d 1-14, q 3 weekly
boolean
C0671970 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
Capecitabine Dosage | Docetaxel Dosage
Item
capecitabine 2000mg/m2 d 1-14, q 3 weekly and docetaxel 75mg/m2 d1 q 3 weekly
boolean
C0671970 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0246415 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Fit Pharmaceutical Preparations Dose Full
Item
fit to start at full (100%) starting dose of all drugs
boolean
C0424576 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0443225 (UMLS CUI [1,4])
Able to operate mobile phone | Use of Mobile Phone Willing
Item
able and willing to use mobile phone
boolean
C4274610 (UMLS CUI [1])
C1524063 (UMLS CUI [2,1])
C1136360 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Renal function | Liver function | Bone Marrow function
Item
reasonable renal, liver and bone marrow function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0005953 (UMLS CUI [3,1])
C0031843 (UMLS CUI [3,2])
Absolute neutrophil count
Item
absolute neutrophil count (anc) >1.5 x 109/l
boolean
C0948762 (UMLS CUI [1])
Platelet Count measurement
Item
platelet count > 100 x 109/l
boolean
C0032181 (UMLS CUI [1])
Serum total bilirubin measurement
Item
total bilirubin <1.5 uln
boolean
C1278039 (UMLS CUI [1])
Alanine aminotransferase measurement | Aspartate aminotransferase measurement
Item
alt, ast < 2.5 x uln
boolean
C0201836 (UMLS CUI [1])
C0201899 (UMLS CUI [2])
Alkaline phosphatase measurement
Item
alkaline phosphatase < 2.5 x uln
boolean
C0201850 (UMLS CUI [1])
Absence Medical contraindication Capecitabine | Absence Medical contraindication Oxaliplatin | Absence Medical contraindication Docetaxel
Item
no obvious contra indications to capecitabine or oxaliplatin or docetaxel
boolean
C0332197 (UMLS CUI [1,1])
C1301624 (UMLS CUI [1,2])
C0671970 (UMLS CUI [1,3])
C0332197 (UMLS CUI [2,1])
C1301624 (UMLS CUI [2,2])
C0069717 (UMLS CUI [2,3])
C0332197 (UMLS CUI [3,1])
C1301624 (UMLS CUI [3,2])
C0246415 (UMLS CUI [3,3])
Able to read English Language | Able to write English Language | Comprehension English Language
Item
patients must also be able to read, write and understand english.
boolean
C0586740 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0233733 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Residence | Mobile Phone Network Lacking | Other Coding
Item
patients who live in an area of no vodafone or orange mobile phone network - -
boolean
C0237096 (UMLS CUI [1])
C1136360 (UMLS CUI [2,1])
C1882071 (UMLS CUI [2,2])
C0332268 (UMLS CUI [2,3])
C3846158 (UMLS CUI [3])
Study Subject Participation Status | Cancer treatment
Item
patients participating in other cancer treatment trials
boolean
C2348568 (UMLS CUI [1])
C0920425 (UMLS CUI [2])
Renal Insufficiency Moderate | Renal Insufficiency Severe | Estimation of creatinine clearance by Cockcroft-Gault formula
Item
moderate or severe renal impairment [creatinine clearance <30ml/min (calculated according to cockroft-gault formula)]
boolean
C1565489 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C1565489 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C2711451 (UMLS CUI [3])

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