ID

22553

Descrição

ODM derived from http://clinicaltrials.gov/show/NCT00275379

Link

http://clinicaltrials.gov/show/NCT00275379

Palavras-chave

  1. 06/03/2012 06/03/2012 -
  2. 07/06/2017 07/06/2017 - Martin Dugas
Transferido a

7 de junho de 2017

DOI

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Licença

Creative Commons BY 4.0

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Study Evaluating Orally Administered ERB-041 in Subjects With Active Interstitial Cystitis

  1. StudyEvent: Eligibility
    1. Eligibility
Einschlusskriterien
Descrição

Einschlusskriterien

Alias
UMLS CUI-1
C1512693
Alter 18 Jahre und älter
Descrição

Legal adult

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1706450
Subjects seeking medical treatment for symptoms consistent with IC that have been ongoing for > 9 months or seeking medical treatment for a previous documented diagnosis of IC
Descrição

Interstitial Cystitis

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0282488
Subjects who are not surgically sterile or postmenopausal (amenorrheic > 12 months) must agree and commit to the use of a medically acceptable, highly-effective (i.e. double-barrier or IUD), non-hormonal form of birth control during the study and for 30 days after the last dose of test
Descrição

birth control

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0700589
Ausschlusskriterien
Descrição

Ausschlusskriterien

Alias
UMLS CUI-1
C0680251
Use of herbal supplements (except for a daily multivitamin/mineral supplement not containing herbal components)
Descrição

Herbal supplements

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1504473
History of cancer (other than resected cutaneous basal or squamous cell carcinoma or in situ cervical cancer) with less than 5 years documentation of a disease-free state
Descrição

History of cancer

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2735088
Vaginitis or vaginal infection within 1 month before randomization
Descrição

Vaginitis or vaginal infection

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0042267
UMLS CUI [1,2]
C0404521

Similar models

Eligibility

  1. StudyEvent: Eligibility
    1. Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Einschlusskriterien
C1512693 (UMLS CUI-1)
Legal adult
Item
Alter 18 Jahre und älter
boolean
C1706450 (UMLS CUI [1])
Interstitial Cystitis
Item
Subjects seeking medical treatment for symptoms consistent with IC that have been ongoing for > 9 months or seeking medical treatment for a previous documented diagnosis of IC
boolean
C0282488 (UMLS CUI [1])
birth control
Item
Subjects who are not surgically sterile or postmenopausal (amenorrheic > 12 months) must agree and commit to the use of a medically acceptable, highly-effective (i.e. double-barrier or IUD), non-hormonal form of birth control during the study and for 30 days after the last dose of test
boolean
C0700589 (UMLS CUI [1])
Item Group
Ausschlusskriterien
C0680251 (UMLS CUI-1)
Herbal supplements
Item
Use of herbal supplements (except for a daily multivitamin/mineral supplement not containing herbal components)
boolean
C1504473 (UMLS CUI [1])
History of cancer
Item
History of cancer (other than resected cutaneous basal or squamous cell carcinoma or in situ cervical cancer) with less than 5 years documentation of a disease-free state
boolean
C2735088 (UMLS CUI [1])
Vaginitis or vaginal infection
Item
Vaginitis or vaginal infection within 1 month before randomization
boolean
C0042267 (UMLS CUI [1,1])
C0404521 (UMLS CUI [1,2])

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