ID

40766

Descripción

Wearable Pulsed Electromagnetic Fields Device in Knee Osteoarthritis: Double Blinded, Randomized Clinical Trial; ODM derived from: https://clinicaltrials.gov/show/NCT01877278

Link

https://clinicaltrials.gov/show/NCT01877278

Palabras clave

Versiones (1)
  1. 9/5/20 9/5/20 -
Titular de derechos de autor

See clinicaltrials.gov

Subido en

9 de mayo de 2020

DOI

Para solicitar uno, por favor iniciar sesión.

Licencia

Creative Commons BY 4.0
Comentarios del modelo :

Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.

Volver a los comentarios del modelo
Comentarios de grupo de elementos para :

Comentarios del elemento para :

Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.

Eligibility Knee Osteoarthritis NCT01877278

Inglés

Eligibility Knee Osteoarthritis NCT01877278

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
a diagnosis of primary oa of the knee according to the acr criteria, including radiologic evidence of oa
Descripción

Primary osteoarthritis of knee | Osteoarthritis Radiology

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2893931
UMLS CUI [2,1]
C0029408
UMLS CUI [2,2]
C0043299
age >40 years
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
symptomatic disease for at least 6 months prior to enrollment
Descripción

Disease Symptomatic Duration

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C0231220
UMLS CUI [1,3]
C0449238
persistent pain despite receiving the maximum tolerated doses of conventional medical therapy, including acetaminophen (4 gm/day) and/or a nonsteroidal antiinflammatory drug (nsaid), with persistent pain defined as a minimum mean score of 25 mm on the visual analog scales (vas) for global pain (0-100-mm range for each) daily pain during the month prior to study enrollment
Descripción

Pain Persistent | Standard therapy Maximum Tolerated Dose | Acetaminophen U/day | Anti-Inflammatory Agents, Non-Steroidal | Pain daily mean Visual Analog Pain Scale

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C0205322
UMLS CUI [2,1]
C2936643
UMLS CUI [2,2]
C0752079
UMLS CUI [3,1]
C0000970
UMLS CUI [3,2]
C0456683
UMLS CUI [4]
C0003211
UMLS CUI [5,1]
C3845611
UMLS CUI [5,2]
C0444504
UMLS CUI [5,3]
C0042815
ability to attend followup appointments
Descripción

Compliance behavior Follow-up

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C3274571
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary causes of oa
Descripción

Secondary osteoarthritis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2732281
local or systemic infection
Descripción

Local infection | Sepsis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1400591
UMLS CUI [2]
C0243026
diabetes mellitus
Descripción

Diabetes Mellitus

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0011849
systemic arthritis
Descripción

Arthritis Systemic

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0003864
UMLS CUI [1,2]
C0205373
allergy to anesthetic agent or contrast material
Descripción

Anesthetic allergy | Contrast media allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0741020
UMLS CUI [2]
C0570562
coagulopathy
Descripción

Blood Coagulation Disorders

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005779
anticoagulant therapy
Descripción

Anticoagulant therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0150457
had previous ia steroid injection
Descripción

Intraarticular steroid injection

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2064783
avascular necrosis of bone
Descripción

Avascular necrosis of bone

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027543
patients who are on specific oa pharmacological therapy (nsaids, opioids) for more than 2 weeks prior enrollment
Descripción

Pharmacotherapy Specific Osteoarthritis | NSAIDs | Opioids

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C0205369
UMLS CUI [1,3]
C0029408
UMLS CUI [2]
C0003211
UMLS CUI [3]
C0242402
Volver a la parte superior de la página

Similar models

Eligibility Knee Osteoarthritis NCT01877278

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Primary osteoarthritis of knee | Osteoarthritis Radiology
Item
a diagnosis of primary oa of the knee according to the acr criteria, including radiologic evidence of oa
boolean
C2893931 (UMLS CUI [1])
C0029408 (UMLS CUI [2,1])
C0043299 (UMLS CUI [2,2])
Age
Item
age >40 years
boolean
C0001779 (UMLS CUI [1])
Disease Symptomatic Duration
Item
symptomatic disease for at least 6 months prior to enrollment
boolean
C0012634 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0449238 (UMLS CUI [1,3])
Pain Persistent | Standard therapy Maximum Tolerated Dose | Acetaminophen U/day | Anti-Inflammatory Agents, Non-Steroidal | Pain daily mean Visual Analog Pain Scale
Item
persistent pain despite receiving the maximum tolerated doses of conventional medical therapy, including acetaminophen (4 gm/day) and/or a nonsteroidal antiinflammatory drug (nsaid), with persistent pain defined as a minimum mean score of 25 mm on the visual analog scales (vas) for global pain (0-100-mm range for each) daily pain during the month prior to study enrollment
boolean
C0030193 (UMLS CUI [1,1])
C0205322 (UMLS CUI [1,2])
C2936643 (UMLS CUI [2,1])
C0752079 (UMLS CUI [2,2])
C0000970 (UMLS CUI [3,1])
C0456683 (UMLS CUI [3,2])
C0003211 (UMLS CUI [4])
C3845611 (UMLS CUI [5,1])
C0444504 (UMLS CUI [5,2])
C0042815 (UMLS CUI [5,3])
Compliance behavior Follow-up
Item
ability to attend followup appointments
boolean
C1321605 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Secondary osteoarthritis
Item
secondary causes of oa
boolean
C2732281 (UMLS CUI [1])
Local infection | Sepsis
Item
local or systemic infection
boolean
C1400591 (UMLS CUI [1])
C0243026 (UMLS CUI [2])
Diabetes Mellitus
Item
diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Arthritis Systemic
Item
systemic arthritis
boolean
C0003864 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
Anesthetic allergy | Contrast media allergy
Item
allergy to anesthetic agent or contrast material
boolean
C0741020 (UMLS CUI [1])
C0570562 (UMLS CUI [2])
Blood Coagulation Disorders
Item
coagulopathy
boolean
C0005779 (UMLS CUI [1])
Anticoagulant therapy
Item
anticoagulant therapy
boolean
C0150457 (UMLS CUI [1])
Intraarticular steroid injection
Item
had previous ia steroid injection
boolean
C2064783 (UMLS CUI [1])
Avascular necrosis of bone
Item
avascular necrosis of bone
boolean
C0027543 (UMLS CUI [1])
Pharmacotherapy Specific Osteoarthritis | NSAIDs | Opioids
Item
patients who are on specific oa pharmacological therapy (nsaids, opioids) for more than 2 weeks prior enrollment
boolean
C0013216 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
C0029408 (UMLS CUI [1,3])
C0003211 (UMLS CUI [2])
C0242402 (UMLS CUI [3])
Volver a la parte superior de la página 

Contacto

Utilice este formulario para comentarios, preguntas y sugerencias.

Los campos marcados con * son obligatorios.

Ayuda

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial