ID

19224

Descripción

The Effectiveness of a Nighttime Positioning Hand Splint in Patients With Rheumatoid Arthritis; ODM derived from: https://clinicaltrials.gov/show/NCT00502424

Link

https://clinicaltrials.gov/show/NCT00502424

Palabras clave

Versiones (1)
  1. 13/12/16 13/12/16 -
Subido en

13 de diciembre de 2016

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis. NCT00502424

Inglés

Eligibility Rheumatoid Arthritis. NCT00502424

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

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

Rheumatoid Arthritis Classification

Tipo de datos

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.
Descripción

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

Tipo de datos

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.
Descripción

Hand Aching Visual Analog Pain Scale

Tipo de datos

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.
Descripción

Study Subject Participation Status agreement | Informed Consent

Tipo de datos

boolean

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

Exclusion Criteria

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

Deformity Hand Aching | Splint Device Manufacturing Problem

Tipo de datos

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.
Descripción

Upper limb Splint Type

Tipo de datos

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.
Descripción

patient scheduled for surgery

Tipo de datos

boolean

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

Hypersensitivity Splint Material

Tipo de datos

boolean

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

Mental deficiency

Tipo de datos

boolean

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

residence Problem

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0033213
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Similar models

Eligibility Rheumatoid Arthritis. NCT00502424

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
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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