ID

40766

Beschrijving

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

Trefwoorden

Versies (1)
  1. 09-05-20 09-05-20 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

9 mei 2020

DOI

Voor een aanvraag inloggen.

Licentie

Creative Commons BY 4.0
Model Commentaren :

Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.

Terug naar het model Commentaren
Itemgroep Commentaren voor :

Item Commentaren voor :

U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.

Eligibility Knee Osteoarthritis NCT01877278

Engels

Eligibility Knee Osteoarthritis NCT01877278

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

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

Primary osteoarthritis of knee | Osteoarthritis Radiology

Datatype

boolean

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

Age

Datatype

boolean

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

Disease Symptomatic Duration

Datatype

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
Beschrijving

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

Datatype

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
Beschrijving

Compliance behavior Follow-up

Datatype

boolean

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

Exclusion Criteria

Alias
UMLS CUI
C0680251
secondary causes of oa
Beschrijving

Secondary osteoarthritis

Datatype

boolean

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

Local infection | Sepsis

Datatype

boolean

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

Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1]
C0011849
systemic arthritis
Beschrijving

Arthritis Systemic

Datatype

boolean

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

Anesthetic allergy | Contrast media allergy

Datatype

boolean

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

Blood Coagulation Disorders

Datatype

boolean

Alias
UMLS CUI [1]
C0005779
anticoagulant therapy
Beschrijving

Anticoagulant therapy

Datatype

boolean

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

Intraarticular steroid injection

Datatype

boolean

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

Avascular necrosis of bone

Datatype

boolean

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

Pharmacotherapy Specific Osteoarthritis | NSAIDs | Opioids

Datatype

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
Terug naar het begin van de pagina

Similar models

Eligibility Knee Osteoarthritis NCT01877278

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
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])
Terug naar het begin van de pagina 

Contact

Gebruik dit formulier voor feedback, vragen en verbeteringsvoorstellen.

Velden gemarkeerd met een * zijn verplicht.

Help

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