ID

13885

Beschrijving

Efficacy of Gabapentin in Prevention of Tourniquet Pain and Hypertension; ODM derived from: https://clinicaltrials.gov/show/NCT01441531

Link

https://clinicaltrials.gov/show/NCT01441531

Trefwoorden

  1. 13-03-16 13-03-16 -
Geüploaded op

13 maart 2016

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Tourniquet-induced Pain NCT01441531

Eligibility Tourniquet-induced Pain NCT01441531

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient ages 18-64
Beschrijving

age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
asa physical status 1-3
Beschrijving

asa physical status

Datatype

boolean

Alias
UMLS CUI [1]
C0450990
schedule for orif tibia fracture with use of pneumatic tourniquet
Beschrijving

orif tibia fracture; pneumatic tourniquet

Datatype

boolean

Alias
UMLS CUI [1]
C0749493
UMLS CUI [2]
C0183980
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
allergy to study medications
Beschrijving

hypersensitivity study drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C0008972
polytrauma
Beschrijving

polytrauma

Datatype

boolean

Alias
UMLS CUI [1]
C0026771
lower extremity crush injury
Beschrijving

lower extremity crush injury

Datatype

boolean

Alias
UMLS CUI [1]
C0745851
chronic opioid use
Beschrijving

chronic opioid use

Datatype

boolean

Alias
UMLS CUI [1]
C0338779
sickle cell disease or trait
Beschrijving

Sickle Cell Trait

Datatype

boolean

Alias
UMLS CUI [1]
C0037054
peripheral vascular disease
Beschrijving

peripheral vascular disease

Datatype

boolean

Alias
UMLS CUI [1]
C0085096
poorly controlled hypertension
Beschrijving

controlled hypertension

Datatype

boolean

Alias
UMLS CUI [1]
C0745117
history of dvt/pe
Beschrijving

Deep Vein Thrombosis

Datatype

boolean

Alias
UMLS CUI [1]
C0149871
morbid obesity (bmi > 35)
Beschrijving

bmi

Datatype

boolean

Alias
UMLS CUI [1]
C1305855
patient or surgeon refusal
Beschrijving

compliance

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
patient inability to properly describe postoperative pain to investigators
Beschrijving

compliance; postoperative pain

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
UMLS CUI [2]
C0030201

Similar models

Eligibility Tourniquet-induced Pain NCT01441531

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
age
Item
patient ages 18-64
boolean
C0001779 (UMLS CUI [1])
asa physical status
Item
asa physical status 1-3
boolean
C0450990 (UMLS CUI [1])
orif tibia fracture; pneumatic tourniquet
Item
schedule for orif tibia fracture with use of pneumatic tourniquet
boolean
C0749493 (UMLS CUI [1])
C0183980 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
hypersensitivity study drugs
Item
allergy to study medications
boolean
C0020517 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C0008972 (UMLS CUI [1,3])
polytrauma
Item
polytrauma
boolean
C0026771 (UMLS CUI [1])
lower extremity crush injury
Item
lower extremity crush injury
boolean
C0745851 (UMLS CUI [1])
chronic opioid use
Item
chronic opioid use
boolean
C0338779 (UMLS CUI [1])
Sickle Cell Trait
Item
sickle cell disease or trait
boolean
C0037054 (UMLS CUI [1])
peripheral vascular disease
Item
peripheral vascular disease
boolean
C0085096 (UMLS CUI [1])
controlled hypertension
Item
poorly controlled hypertension
boolean
C0745117 (UMLS CUI [1])
Deep Vein Thrombosis
Item
history of dvt/pe
boolean
C0149871 (UMLS CUI [1])
bmi
Item
morbid obesity (bmi > 35)
boolean
C1305855 (UMLS CUI [1])
compliance
Item
patient or surgeon refusal
boolean
C1321605 (UMLS CUI [1])
compliance; postoperative pain
Item
patient inability to properly describe postoperative pain to investigators
boolean
C1321605 (UMLS CUI [1])
C0030201 (UMLS CUI [2])

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