Informações:
Falhas:
ID
13085
Descrição
Oral Collagen for Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00000401
Link
https://clinicaltrials.gov/show/NCT00000401
Palavras-chave
Versões (1)
- 15/01/2016 15/01/2016 -
Titular dos direitos
CC BY-NC 3.0
Transferido a
15 de janeiro de 2016
DOI
Para um pedido faça login.
Licença
Creative Commons BY-NC 3.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Rheumatoid Arthritis NCT00000401
Eligibility Rheumatoid Arthritis NCT00000401
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00000401
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
rheumatoid arthritis
Item
clinically stable ra and unlikely to require adjustment of doses of dmards, nsaids, prednisone, or anti-tnfα therapies for the treatment phase of the study
boolean
C0003873 (UMLS CUI [1])
acr criteria
Item
meets american college of rheumatology (acr) 1988 revised criteria for ra
boolean
C0003873 (UMLS CUI [1])
onset of disease at age 16 or older
Item
onset of disease at age 16 or older
boolean
C0277793 (UMLS CUI [1])
onset of disease at least 3 months prior to enrollment
Item
onset of disease at least 3 months prior to enrollment
boolean
C0277793 (UMLS CUI [1])
pbmc - ifnγ - α1(ii)/pbs stimulation index
Item
pbmc - ifnγ - α1(ii)/pbs stimulation index greater than or equal to 1.5 in 6 months prior to baseline visit
boolean
herbal drug
Item
agree to discontinue herbal remedies described in this protocol
boolean
C1360419 (UMLS CUI [1])
contraception
Item
agree to use acceptable forms of contraception
boolean
C0700589 (UMLS CUI [1])
participation in another clinical research study
Item
participation in another clinical research study involving the evaluation of another investigational drug within 90 days prior to study entry
boolean
C2348568 (UMLS CUI [1])
prednisone
Item
currently taking greater than 7.5 mg prednisone daily
boolean
C0032952 (UMLS CUI [1])
intra-articular corticosteroid injections
Item
intra-articular corticosteroid injections within 30 days prior to study entry
boolean
C2064783 (UMLS CUI [1])
concurrent serious medical condition which, in the opinion of the investigator, makes the patient inappropriate for the study
Item
concurrent serious medical condition which, in the opinion of the investigator, makes the patient inappropriate for the study
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
beef allergy
Item
beef allergy
boolean
C0020517 (UMLS CUI [1,1])
C0452849 (UMLS CUI [1,2])
C0452849 (UMLS CUI [1,2])
fish oil
Item
use of fish oil within 4 weeks of study entry
boolean
C0556145 (UMLS CUI [1])
auranofin or cyclophosphamide
Item
previous use of auranofin or cyclophosphamide (all other dmards are allowed)
boolean
C0004320 (UMLS CUI [1])
C0010583 (UMLS CUI [2])
C0010583 (UMLS CUI [2])
stem cell transplantation
Item
previous autologous or heterologous stem cell transplantation
boolean
C1504389 (UMLS CUI [1])
malignancy
Item
active malignancy or past treatment consisting of antineoplastic drugs or total lymphoid irradiation
boolean
C0006826 (UMLS CUI [1])
citrus juice
Item
intolerance to citrus juices or colorless carbonated beverages
boolean
C0020517 (UMLS CUI [1,1])
C2347777 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0007025 (UMLS CUI [2,2])
C2347777 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0007025 (UMLS CUI [2,2])