Information:
Error:
ID
31836
Description
A Study Evaluating the Safety and Efficacy of Cura-100 in Subjects With Rheumatoid Arthritis and Osteoarthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00455208
Link
https://clinicaltrials.gov/show/NCT00455208
Keywords
Versions (1)
- 10/1/18 10/1/18 -
Copyright Holder
See clinicaltrials.gov
Uploaded on
October 1, 2018
DOI
To request one please log in.
License
Creative Commons BY 4.0
Model comments :
You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.
Itemgroup comments for :
Item comments for :
In order to download data models you must be logged in. Please log in or register for free.
Eligibility Rheumatoid Arthritis NCT00455208
Eligibility Rheumatoid Arthritis NCT00455208
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00455208
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Rheumatoid Arthritis | Osteoarthritis
Item
having a diagnosis of rheumatoid arthritis and osteoarthritis at active stage
boolean
C0003873 (UMLS CUI [1])
C0029408 (UMLS CUI [2])
C0029408 (UMLS CUI [2])
Protocol Compliance
Item
able and willing to comply with study visits and procedures specified in this protocol for at least six months period
boolean
C0525058 (UMLS CUI [1])
Informed Consent
Item
able to understand and willing to sign and date the written informed consent form prior to admission of the study
boolean
C0021430 (UMLS CUI [1])
Consent for release of information
Item
able and willing to provide adequate information for locator purposes
boolean
C0511175 (UMLS CUI [1])
Self-Evaluation Information | Diagnostic report Arthritis | Evaluation
Item
able and willing to provide self evaluation information and diagnostic report of arthritis as required for efficacy evaluation
boolean
C2936633 (UMLS CUI [1,1])
C1533716 (UMLS CUI [1,2])
C0498033 (UMLS CUI [2,1])
C0003864 (UMLS CUI [2,2])
C0220825 (UMLS CUI [3])
C1533716 (UMLS CUI [1,2])
C0498033 (UMLS CUI [2,1])
C0003864 (UMLS CUI [2,2])
C0220825 (UMLS CUI [3])
Pregnancy
Item
pregnant women
boolean
C0032961 (UMLS CUI [1])
Overweight
Item
over-weighted
boolean
C0497406 (UMLS CUI [1])
Hypertensive disease | Diabetes Mellitus | Cardiovascular Disease | Kidney Disease | Cutaneous hypersensitivity Serious | Comorbidity Study Subject Participation Status At risk | Medical condition Study Subject Participation Status At risk | Exception Arthritis
Item
hypertension, or diabetes, or a history of cardiovascular disease or kidney disease, or serious skin allergy or other concurrent clinically significant illness or medical condition (other than arthritis) which, in the viewpoint of the study doctor, may put the subject at a possible risk for participation
boolean
C0020538 (UMLS CUI [1])
C0011849 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0585186 (UMLS CUI [5,1])
C0205404 (UMLS CUI [5,2])
C0009488 (UMLS CUI [6,1])
C2348568 (UMLS CUI [6,2])
C1444641 (UMLS CUI [6,3])
C3843040 (UMLS CUI [7,1])
C2348568 (UMLS CUI [7,2])
C1444641 (UMLS CUI [7,3])
C1705847 (UMLS CUI [8,1])
C0003864 (UMLS CUI [8,2])
C0011849 (UMLS CUI [2])
C0007222 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
C0585186 (UMLS CUI [5,1])
C0205404 (UMLS CUI [5,2])
C0009488 (UMLS CUI [6,1])
C2348568 (UMLS CUI [6,2])
C1444641 (UMLS CUI [6,3])
C3843040 (UMLS CUI [7,1])
C2348568 (UMLS CUI [7,2])
C1444641 (UMLS CUI [7,3])
C1705847 (UMLS CUI [8,1])
C0003864 (UMLS CUI [8,2])
Biological Response Modifiers | Immunosuppressive Agents
Item
patients used biologic modifier therapy or currently taking immunosuppressive agents might be excluded
boolean
C0005525 (UMLS CUI [1])
C0021081 (UMLS CUI [2])
C0021081 (UMLS CUI [2])
Therapeutic procedure Medical center Unable
Item
unable to spend 3 hours for treatment at the study center
boolean
C0087111 (UMLS CUI [1,1])
C0565990 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C0565990 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])