ID

38227

Beschreibung

The Efficacy of Acupuncture in Treating Chemotherapy Side Effects in Breast Cancer Patients; ODM derived from: https://clinicaltrials.gov/show/NCT01996410

Link

https://clinicaltrials.gov/show/NCT01996410

Stichworte

Versionen (1)
  1. 29.09.19 29.09.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

29. September 2019

DOI

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Creative Commons BY 4.0
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Eligibility Breast Cancer Stages I Through III NCT01996410

Englisch

Eligibility Breast Cancer Stages I Through III NCT01996410

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years or older
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
english speaking/reading/writing
Beschreibung

Able to speak English Language | Able to read English Language | Able to write English Language

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0564215
UMLS CUI [1,2]
C0376245
UMLS CUI [2,1]
C0586740
UMLS CUI [2,2]
C0376245
UMLS CUI [3,1]
C0584993
UMLS CUI [3,2]
C0376245
breast cancer stages i through iii
Beschreibung

Breast Carcinoma TNM Breast tumor staging

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0474926
any performance status suitable for chemotherapy as determined by the physician
Beschreibung

Performance status Suitable Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1518965
UMLS CUI [1,2]
C3900053
UMLS CUI [1,3]
C0392920
primary or secondary chemotherapy, but enrolling patients prior to a chemotherapy regimen regardless of previous radiation therapy exposure and/or previous mastectomy.
Beschreibung

Chemotherapy Primary | Chemotherapy Secondary

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0205225
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0175668
scheduled to receive either of the following two regimens:
Beschreibung

Regimen Scheduled

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0040808
UMLS CUI [1,2]
C0205539
adriamycin (60 mg/m2), cytoxan (600 mg/m2), taxol (175 mg/m2)
Beschreibung

Adriamycin Dosage | Cytoxan Dosage | Taxol Dosage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0085752
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0699319
UMLS CUI [2,2]
C0178602
UMLS CUI [3,1]
C0678133
UMLS CUI [3,2]
C0178602
adriamycin (60 mg/m2), cytoxan (600 mg/m2), taxol (80 g/m2)
Beschreibung

Adriamycin Dosage | Cytoxan Dosage | Taxol Dosage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0085752
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0699319
UMLS CUI [2,2]
C0178602
UMLS CUI [3,1]
C0678133
UMLS CUI [3,2]
C0178602
taxotere (75mg/m2), cytoxan (600 mg/m2)
Beschreibung

Taxotere Dosage | Cytoxan Dosage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0699967
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0699319
UMLS CUI [2,2]
C0178602
taxotere (75 mg/m2), carboplatin (auc 6), perjeta (840 mg loading fixed dose, followed by 420 mg maintenance fixed dose)
Beschreibung

Taxotere Dosage | Carboplatin AUC | Perjeta Dosage

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0699967
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0079083
UMLS CUI [2,2]
C0376690
UMLS CUI [3,1]
C3473371
UMLS CUI [3,2]
C0178602
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of narcolepsy
Beschreibung

Narcolepsy

Datentyp

boolean

Alias
UMLS CUI [1]
C0027404
sleep apnea requiring cpap
Beschreibung

Sleep Apnea Requirement CPAP

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0037315
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0199451
other acupuncture treatment within one month of enrollment
Beschreibung

Acupuncture

Datentyp

boolean

Alias
UMLS CUI [1]
C0394664
acupuncture treatment for chemotherapy in the past
Beschreibung

Acupuncture Associated with Chemotherapy

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0394664
UMLS CUI [1,2]
C0332281
UMLS CUI [1,3]
C0392920
current participation in any other research studies
Beschreibung

Study Subject Participation Status | Research study

Datentyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0681814
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Ähnliche Modelle

Eligibility Breast Cancer Stages I Through III NCT01996410

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18 years or older
boolean
C0001779 (UMLS CUI [1])
Able to speak English Language | Able to read English Language | Able to write English Language
Item
english speaking/reading/writing
boolean
C0564215 (UMLS CUI [1,1])
C0376245 (UMLS CUI [1,2])
C0586740 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C0584993 (UMLS CUI [3,1])
C0376245 (UMLS CUI [3,2])
Breast Carcinoma TNM Breast tumor staging
Item
breast cancer stages i through iii
boolean
C0678222 (UMLS CUI [1,1])
C0474926 (UMLS CUI [1,2])
Performance status Suitable Chemotherapy
Item
any performance status suitable for chemotherapy as determined by the physician
boolean
C1518965 (UMLS CUI [1,1])
C3900053 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Chemotherapy Primary | Chemotherapy Secondary
Item
primary or secondary chemotherapy, but enrolling patients prior to a chemotherapy regimen regardless of previous radiation therapy exposure and/or previous mastectomy.
boolean
C0392920 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0175668 (UMLS CUI [2,2])
Regimen Scheduled
Item
scheduled to receive either of the following two regimens:
boolean
C0040808 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
Adriamycin Dosage | Cytoxan Dosage | Taxol Dosage
Item
adriamycin (60 mg/m2), cytoxan (600 mg/m2), taxol (175 mg/m2)
boolean
C0085752 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0699319 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0678133 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
Adriamycin Dosage | Cytoxan Dosage | Taxol Dosage
Item
adriamycin (60 mg/m2), cytoxan (600 mg/m2), taxol (80 g/m2)
boolean
C0085752 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0699319 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0678133 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
Taxotere Dosage | Cytoxan Dosage
Item
taxotere (75mg/m2), cytoxan (600 mg/m2)
boolean
C0699967 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0699319 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
Taxotere Dosage | Carboplatin AUC | Perjeta Dosage
Item
taxotere (75 mg/m2), carboplatin (auc 6), perjeta (840 mg loading fixed dose, followed by 420 mg maintenance fixed dose)
boolean
C0699967 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0079083 (UMLS CUI [2,1])
C0376690 (UMLS CUI [2,2])
C3473371 (UMLS CUI [3,1])
C0178602 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Narcolepsy
Item
history of narcolepsy
boolean
C0027404 (UMLS CUI [1])
Sleep Apnea Requirement CPAP
Item
sleep apnea requiring cpap
boolean
C0037315 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0199451 (UMLS CUI [1,3])
Acupuncture
Item
other acupuncture treatment within one month of enrollment
boolean
C0394664 (UMLS CUI [1])
Acupuncture Associated with Chemotherapy
Item
acupuncture treatment for chemotherapy in the past
boolean
C0394664 (UMLS CUI [1,1])
C0332281 (UMLS CUI [1,2])
C0392920 (UMLS CUI [1,3])
Study Subject Participation Status | Research study
Item
current participation in any other research studies
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2])
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