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Eligibility Rheumatoid Arthritis. NCT00502424

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Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
rheumatoid arthritis classified according to the acr criteria.
Beschrijving

Rheumatoid Arthritis Classification

Datatype

boolean

Alias
UMLS CUI [1,1]
C0003873
UMLS CUI [1,2]
C0008902
use of the same remissive drugs for at least 6 months before the intervention and the same doses of the same corticosteroids and nonsteroidal anti-inflammatory drugs for at least one month before the study.
Beschrijving

Pharmaceutical Preparations Causing Remission | Adrenal Cortex Hormones | Anti-Inflammatory Agents, Non-Steroidal

Datatype

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C0678227
UMLS CUI [1,3]
C0544452
UMLS CUI [2]
C0001617
UMLS CUI [3]
C0003211
a score ≥ 3 and ≤ 7 on a visual analog scale (vas) for pain in the more aching hand.
Beschrijving

Hand Aching Visual Analog Pain Scale

Datatype

boolean

Alias
UMLS CUI [1,1]
C0018563
UMLS CUI [1,2]
C0234238
UMLS CUI [1,3]
C0042815
agreement to participate in the study, and signing of a free informed consent form.
Beschrijving

Study Subject Participation Status agreement | Informed Consent

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0680240
UMLS CUI [2]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
presented deformities in the more aching hand that did not permit fabrication of the splint.
Beschrijving

Deformity Hand Aching | Splint Device Manufacturing Problem

Datatype

boolean

Alias
UMLS CUI [1,1]
C0302142
UMLS CUI [1,2]
C0018563
UMLS CUI [1,3]
C0234238
UMLS CUI [2,1]
C0038009
UMLS CUI [2,2]
C0870840
UMLS CUI [2,3]
C0033213
patients using any other type of upper limb splint.
Beschrijving

Upper limb Splint Type

Datatype

boolean

Alias
UMLS CUI [1,1]
C1140618
UMLS CUI [1,2]
C0038009
UMLS CUI [1,3]
C0332307
patients with a surgery scheduled within 6 months after the study.
Beschrijving

patient scheduled for surgery

Datatype

boolean

Alias
UMLS CUI [1]
C3242215
patients allergic to the splint material.
Beschrijving

Hypersensitivity Splint Material

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0038009
UMLS CUI [1,3]
C0520510
patients with mental deficiency.
Beschrijving

Mental deficiency

Datatype

boolean

Alias
UMLS CUI [1]
C0917816
patients who lived in inaccessible areas.
Beschrijving

residence Problem

Datatype

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0033213
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Eligibility Rheumatoid Arthritis. NCT00502424

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Rheumatoid Arthritis Classification
Item
rheumatoid arthritis classified according to the acr criteria.
boolean
C0003873 (UMLS CUI [1,1])
C0008902 (UMLS CUI [1,2])
Pharmaceutical Preparations Causing Remission | Adrenal Cortex Hormones | Anti-Inflammatory Agents, Non-Steroidal
Item
use of the same remissive drugs for at least 6 months before the intervention and the same doses of the same corticosteroids and nonsteroidal anti-inflammatory drugs for at least one month before the study.
boolean
C0013227 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0544452 (UMLS CUI [1,3])
C0001617 (UMLS CUI [2])
C0003211 (UMLS CUI [3])
Hand Aching Visual Analog Pain Scale
Item
a score ≥ 3 and ≤ 7 on a visual analog scale (vas) for pain in the more aching hand.
boolean
C0018563 (UMLS CUI [1,1])
C0234238 (UMLS CUI [1,2])
C0042815 (UMLS CUI [1,3])
Study Subject Participation Status agreement | Informed Consent
Item
agreement to participate in the study, and signing of a free informed consent form.
boolean
C2348568 (UMLS CUI [1,1])
C0680240 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Deformity Hand Aching | Splint Device Manufacturing Problem
Item
presented deformities in the more aching hand that did not permit fabrication of the splint.
boolean
C0302142 (UMLS CUI [1,1])
C0018563 (UMLS CUI [1,2])
C0234238 (UMLS CUI [1,3])
C0038009 (UMLS CUI [2,1])
C0870840 (UMLS CUI [2,2])
C0033213 (UMLS CUI [2,3])
Upper limb Splint Type
Item
patients using any other type of upper limb splint.
boolean
C1140618 (UMLS CUI [1,1])
C0038009 (UMLS CUI [1,2])
C0332307 (UMLS CUI [1,3])
patient scheduled for surgery
Item
patients with a surgery scheduled within 6 months after the study.
boolean
C3242215 (UMLS CUI [1])
Hypersensitivity Splint Material
Item
patients allergic to the splint material.
boolean
C0020517 (UMLS CUI [1,1])
C0038009 (UMLS CUI [1,2])
C0520510 (UMLS CUI [1,3])
Mental deficiency
Item
patients with mental deficiency.
boolean
C0917816 (UMLS CUI [1])
residence Problem
Item
patients who lived in inaccessible areas.
boolean
C0237096 (UMLS CUI [1,1])
C0033213 (UMLS CUI [1,2])
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