Information:
Fel:
ID
22553
Beskrivning
ODM derived from http://clinicaltrials.gov/show/NCT00275379
Länk
http://clinicaltrials.gov/show/NCT00275379
Nyckelord
Versioner (2)
- 2012-03-06 2012-03-06 -
- 2017-06-07 2017-06-07 - Martin Dugas
Uppladdad den
7 juni 2017
DOI
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Licens
Creative Commons BY 4.0
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Study Evaluating Orally Administered ERB-041 in Subjects With Active Interstitial Cystitis
Similar models
Eligibility
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
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])
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])
C0404521 (UMLS CUI [1,2])