ID

38163

Description

Effectiveness of Accelerated Intervention With Compression Sleeve in Mild and Moderate Breast Cancer-related Lymphedema; ODM derived from: https://clinicaltrials.gov/show/NCT01954654

Link

https://clinicaltrials.gov/show/NCT01954654

Keywords

  1. 9/23/19 9/23/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 23, 2019

DOI

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License

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT01954654

Eligibility Breast Cancer NCT01954654

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
participants must be refered for the first time due to unilateral arm lymphedema secondary to primary unilateral breast cancer treatment
Description

Edema of the upper extremity Unilateral | Secondary to Unilateral Breast Carcinoma Treatment

Data type

boolean

Alias
UMLS CUI [1,1]
C0522035
UMLS CUI [1,2]
C0205092
UMLS CUI [2,1]
C0175668
UMLS CUI [2,2]
C1710547
UMLS CUI [2,3]
C0087111
participants must be ≥ 2 months after chemo- and radiotherapy
Description

Status post Chemotherapy | Status post Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C0231290
UMLS CUI [1,2]
C0392920
UMLS CUI [2,1]
C0231290
UMLS CUI [2,2]
C1522449
participants must have elv ≥10% and < 30% and/or > 2 cm difference between the circumference of the two arms at minimum one circumference due to lymphedema
Description

Excess Volume of upper limb | Circumference of arm Due to Lymphedema

Data type

boolean

Alias
UMLS CUI [1,1]
C1979886
UMLS CUI [1,2]
C2959472
UMLS CUI [2,1]
C2075184
UMLS CUI [2,2]
C0678226
UMLS CUI [2,3]
C0024236
participants must be motivated for treatment with compression sleeve and -gauntlet
Description

Treatment Compression Sleeve | Treatment Compression Gauntlet

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0728907
UMLS CUI [1,3]
C0183336
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0728907
UMLS CUI [2,3]
C1289826
participants live in and around aarhus, denmark
Description

Residence Denmark

Data type

boolean

Alias
UMLS CUI [1,1]
C0237096
UMLS CUI [1,2]
C0011318
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
known metastatic disease
Description

Neoplasm Metastasis

Data type

boolean

Alias
UMLS CUI [1]
C0027627
contraindication for treatment with compression sleeve
Description

Medical contraindication Treatment Compression Sleeve

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0087111
UMLS CUI [1,3]
C0728907
UMLS CUI [1,4]
C0183336
upper extremity deep venous thrombosis
Description

Upper Extremity Deep Vein Thrombosis

Data type

boolean

Alias
UMLS CUI [1]
C2717899
previously use of compression sleeve
Description

Use of Compression Sleeve Previous

Data type

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C0728907
UMLS CUI [1,3]
C0183336
UMLS CUI [1,4]
C0205156
known contact allergy to latex
Description

Latex allergy

Data type

boolean

Alias
UMLS CUI [1]
C0577628
unable to fill in questionnaire and/or comply with treatment due to lacking danish language skills, mental state or psychological condition
Description

Questionnaire Completion Unable | Treatment Compliance Unable | Language skills Danish Lacking | Abnormal mental state | Psychological impairment

Data type

boolean

Alias
UMLS CUI [1,1]
C0034394
UMLS CUI [1,2]
C0205197
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C4319828
UMLS CUI [2,2]
C1299582
UMLS CUI [3,1]
C1145677
UMLS CUI [3,2]
C0010969
UMLS CUI [3,3]
C0332268
UMLS CUI [4]
C0278061
UMLS CUI [5]
C0848772

Similar models

Eligibility Breast Cancer NCT01954654

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Edema of the upper extremity Unilateral | Secondary to Unilateral Breast Carcinoma Treatment
Item
participants must be refered for the first time due to unilateral arm lymphedema secondary to primary unilateral breast cancer treatment
boolean
C0522035 (UMLS CUI [1,1])
C0205092 (UMLS CUI [1,2])
C0175668 (UMLS CUI [2,1])
C1710547 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,3])
Status post Chemotherapy | Status post Therapeutic radiology procedure
Item
participants must be ≥ 2 months after chemo- and radiotherapy
boolean
C0231290 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0231290 (UMLS CUI [2,1])
C1522449 (UMLS CUI [2,2])
Excess Volume of upper limb | Circumference of arm Due to Lymphedema
Item
participants must have elv ≥10% and < 30% and/or > 2 cm difference between the circumference of the two arms at minimum one circumference due to lymphedema
boolean
C1979886 (UMLS CUI [1,1])
C2959472 (UMLS CUI [1,2])
C2075184 (UMLS CUI [2,1])
C0678226 (UMLS CUI [2,2])
C0024236 (UMLS CUI [2,3])
Treatment Compression Sleeve | Treatment Compression Gauntlet
Item
participants must be motivated for treatment with compression sleeve and -gauntlet
boolean
C0087111 (UMLS CUI [1,1])
C0728907 (UMLS CUI [1,2])
C0183336 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C0728907 (UMLS CUI [2,2])
C1289826 (UMLS CUI [2,3])
Residence Denmark
Item
participants live in and around aarhus, denmark
boolean
C0237096 (UMLS CUI [1,1])
C0011318 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis
Item
known metastatic disease
boolean
C0027627 (UMLS CUI [1])
Medical contraindication Treatment Compression Sleeve
Item
contraindication for treatment with compression sleeve
boolean
C1301624 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
C0728907 (UMLS CUI [1,3])
C0183336 (UMLS CUI [1,4])
Upper Extremity Deep Vein Thrombosis
Item
upper extremity deep venous thrombosis
boolean
C2717899 (UMLS CUI [1])
Use of Compression Sleeve Previous
Item
previously use of compression sleeve
boolean
C1524063 (UMLS CUI [1,1])
C0728907 (UMLS CUI [1,2])
C0183336 (UMLS CUI [1,3])
C0205156 (UMLS CUI [1,4])
Latex allergy
Item
known contact allergy to latex
boolean
C0577628 (UMLS CUI [1])
Questionnaire Completion Unable | Treatment Compliance Unable | Language skills Danish Lacking | Abnormal mental state | Psychological impairment
Item
unable to fill in questionnaire and/or comply with treatment due to lacking danish language skills, mental state or psychological condition
boolean
C0034394 (UMLS CUI [1,1])
C0205197 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C4319828 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C1145677 (UMLS CUI [3,1])
C0010969 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
C0278061 (UMLS CUI [4])
C0848772 (UMLS CUI [5])

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