ID

23477

Descripción

Safety and Tolerability of 4975 in the Treatment of Moderate to Severe Knee Pain Due to Osteoarthritis (OA); ODM derived from: https://clinicaltrials.gov/show/NCT00667654

Link

https://clinicaltrials.gov/show/NCT00667654

Palabras clave

  1. 7/7/17 7/7/17 -
Subido en

7 de julio de 2017

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Osteoarthritis of the Knee NCT00667654

Eligibility Osteoarthritis of the Knee NCT00667654

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female patients aged 40 years or over.
Descripción

ID.1

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
body mass index (bmi) of 35 or less.
Descripción

ID.2

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1305855
history of oa of the knee for at least 1 year and has experienced pain in the target area for at least six months.
Descripción

ID.3

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0409959
x-ray of the target knee.
Descripción

ID.4

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0203273
willing and able to complete the study procedures.
Descripción

ID.5

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
female patients who are pregnant or lactating or who plan to get pregnant.
Descripción

ID.6

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
clinically significant form of joint disease other than oa.
Descripción

ID.7

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0022408
medical condition that could adversely impact the patient's participation, safety or affect the conduct of the study.
Descripción

ID.8

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0012634
prior major trauma in the target knee or major surgeries such as partial or total knee arthroplasty.
Descripción

ID.9

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332677
UMLS CUI [1,2]
C0679637
UMLS CUI [1,3]
C0022742
arthroscopic surgery on the target knee within 6 months.
Descripción

ID.10

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0022742
UMLS CUI [1,2]
C0750934

Similar models

Eligibility Osteoarthritis of the Knee NCT00667654

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
male or female patients aged 40 years or over.
boolean
C0001779 (UMLS CUI [1])
ID.2
Item
body mass index (bmi) of 35 or less.
boolean
C1305855 (UMLS CUI [1])
ID.3
Item
history of oa of the knee for at least 1 year and has experienced pain in the target area for at least six months.
boolean
C0409959 (UMLS CUI [1])
ID.4
Item
x-ray of the target knee.
boolean
C0203273 (UMLS CUI [1])
ID.5
Item
willing and able to complete the study procedures.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.6
Item
female patients who are pregnant or lactating or who plan to get pregnant.
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
ID.7
Item
clinically significant form of joint disease other than oa.
boolean
C0022408 (UMLS CUI [1])
ID.8
Item
medical condition that could adversely impact the patient's participation, safety or affect the conduct of the study.
boolean
C0012634 (UMLS CUI [1])
ID.9
Item
prior major trauma in the target knee or major surgeries such as partial or total knee arthroplasty.
boolean
C0332677 (UMLS CUI [1,1])
C0679637 (UMLS CUI [1,2])
C0022742 (UMLS CUI [1,3])
ID.10
Item
arthroscopic surgery on the target knee within 6 months.
boolean
C0022742 (UMLS CUI [1,1])
C0750934 (UMLS CUI [1,2])

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