ID

19679

Beschrijving

Phase 3 Study of Acupression's Bracelets in Nausea and Vomiting Induced by FEC100 Chemotherapy's Sort.; ODM derived from: https://clinicaltrials.gov/show/NCT00268125

Link

https://clinicaltrials.gov/show/NCT00268125

Trefwoorden

  1. 21-01-17 21-01-17 -
Geüploaded op

21 januari 2017

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0

Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Breast Neoplasms NCT00268125

Eligibility Breast Neoplasms NCT00268125

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
woman
Beschrijving

Gender

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
age > 18 years
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
well-informed written consent, signed by the patient before the beginning of the study
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
breast cancer's diagnosis (operated or not)
Beschrijving

Breast Carcinoma | Breast Carcinoma Resected

Datatype

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C1521996
forecast of a treatment by fec100 chemotherapy's sort (d1=d21) during at least 3 cycles.
Beschrijving

Chemotherapy cycle Quantity FEC 100

Datatype

boolean

Alias
UMLS CUI [1,1]
C1302181
UMLS CUI [1,2]
C1265611
UMLS CUI [1,3]
C0060133
patient affiliated at a welfare or beneficiary from it
Beschrijving

Welfare Affiliated | Beneficiary Affiliated

Datatype

boolean

Alias
UMLS CUI [1,1]
C0037440
UMLS CUI [1,2]
C1510826
UMLS CUI [2,1]
C1550502
UMLS CUI [2,2]
C1510826
investigator estimates that the patient is able to conform with protocol's conditions and to respect them
Beschrijving

Protocol Compliance

Datatype

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
operated arm's lymphedema
Beschrijving

Lymphedema of arm Operative Surgical Procedure Related

Datatype

boolean

Alias
UMLS CUI [1,1]
C0730207
UMLS CUI [1,2]
C0543467
UMLS CUI [1,3]
C0439849
wrist's morphology which cannot permit the bracelet's wearing (20 cm)
Beschrijving

Wrist Morphology | Medical Identification Bracelet Inappropriate

Datatype

boolean

Alias
UMLS CUI [1,1]
C0043262
UMLS CUI [1,2]
C0332437
UMLS CUI [2,1]
C2355953
UMLS CUI [2,2]
C1548788
d1=d15 fec100's treatment
Beschrijving

Therapeutic procedure FEC 100

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0060133
psychic incapability to sign a well-informed consent
Beschrijving

Informed Consent incapable

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1550518
refusal to give a written consent
Beschrijving

Informed Consent Refused

Datatype

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1705116
patient under tutelage or guardianship
Beschrijving

Patient guardianship

Datatype

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0870627
pregnant or breast-feeding woman
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
any clinical trial's participation which would impose nausea and vomiting's treatment modalities
Beschrijving

Therapeutic procedure Modality Nausea | Therapeutic procedure Modality Vomiting

Datatype

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0695347
UMLS CUI [1,3]
C0027497
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0695347
UMLS CUI [2,3]
C0042963

Similar models

Eligibility Breast Neoplasms NCT00268125

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender
Item
woman
boolean
C0079399 (UMLS CUI [1])
Age
Item
age > 18 years
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
well-informed written consent, signed by the patient before the beginning of the study
boolean
C0021430 (UMLS CUI [1])
Breast Carcinoma | Breast Carcinoma Resected
Item
breast cancer's diagnosis (operated or not)
boolean
C0678222 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C1521996 (UMLS CUI [2,2])
Chemotherapy cycle Quantity FEC 100
Item
forecast of a treatment by fec100 chemotherapy's sort (d1=d21) during at least 3 cycles.
boolean
C1302181 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C0060133 (UMLS CUI [1,3])
Welfare Affiliated | Beneficiary Affiliated
Item
patient affiliated at a welfare or beneficiary from it
boolean
C0037440 (UMLS CUI [1,1])
C1510826 (UMLS CUI [1,2])
C1550502 (UMLS CUI [2,1])
C1510826 (UMLS CUI [2,2])
Protocol Compliance
Item
investigator estimates that the patient is able to conform with protocol's conditions and to respect them
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Lymphedema of arm Operative Surgical Procedure Related
Item
operated arm's lymphedema
boolean
C0730207 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,3])
Wrist Morphology | Medical Identification Bracelet Inappropriate
Item
wrist's morphology which cannot permit the bracelet's wearing (20 cm)
boolean
C0043262 (UMLS CUI [1,1])
C0332437 (UMLS CUI [1,2])
C2355953 (UMLS CUI [2,1])
C1548788 (UMLS CUI [2,2])
Therapeutic procedure FEC 100
Item
d1=d15 fec100's treatment
boolean
C0087111 (UMLS CUI [1,1])
C0060133 (UMLS CUI [1,2])
Informed Consent incapable
Item
psychic incapability to sign a well-informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1550518 (UMLS CUI [1,2])
Informed Consent Refused
Item
refusal to give a written consent
boolean
C0021430 (UMLS CUI [1,1])
C1705116 (UMLS CUI [1,2])
Patient guardianship
Item
patient under tutelage or guardianship
boolean
C0030705 (UMLS CUI [1,1])
C0870627 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or breast-feeding woman
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Therapeutic procedure Modality Nausea | Therapeutic procedure Modality Vomiting
Item
any clinical trial's participation which would impose nausea and vomiting's treatment modalities
boolean
C0087111 (UMLS CUI [1,1])
C0695347 (UMLS CUI [1,2])
C0027497 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C0695347 (UMLS CUI [2,2])
C0042963 (UMLS CUI [2,3])

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial