ID

36697

Description

Standard Versus PICO Dressings in Lower-Extremity Bypass Patients; ODM derived from: https://clinicaltrials.gov/show/NCT02492854

Link

https://clinicaltrials.gov/show/NCT02492854

Keywords

  1. 6/2/19 6/2/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 2, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Of Bypass Graft of the Extremities NCT02492854

Eligibility Of Bypass Graft of the Extremities NCT02492854

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age > 35 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
patient to undergo lower extremity bypass using ipsilateral great saphenous vein harvest
Description

Lower Extremity Bypass | Harvest Great saphenous vein Ipsilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C0023216
UMLS CUI [1,2]
C0741847
UMLS CUI [2,1]
C1512335
UMLS CUI [2,2]
C1278976
UMLS CUI [2,3]
C0441989
willing to comply with protocol, attend follow-up appointments, complete all study assessments, and provide written informed consent.
Description

Protocol Compliance | Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0525058
UMLS CUI [2]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who received an investigational drug for peripheral arterial disease within 4 weeks of screening or who participated in another non-observational clinical trial in the prior 30 days
Description

Investigational New Drugs Peripheral Arterial Disease | Study Subject Participation Status Interventional Study

Data type

boolean

Alias
UMLS CUI [1,1]
C0013230
UMLS CUI [1,2]
C1704436
UMLS CUI [2,1]
C2348568
UMLS CUI [2,2]
C3274035
inability or refusal to provide informed consent
Description

Informed Consent Unable | Informed Consent Refused

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1705116
pregnancy or lactation
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
current immune-suppressive medication, chemotherapy, or radiation therapy
Description

Immunosuppressive Agents | Chemotherapy | Therapeutic radiology procedure

Data type

boolean

Alias
UMLS CUI [1]
C0021081
UMLS CUI [2]
C0392920
UMLS CUI [3]
C1522449
any infrainguinal revascularization procedure on index leg within 12 weeks prior to treatment
Description

Revascularization Inguinal Leg Involved

Data type

boolean

Alias
UMLS CUI [1,1]
C0581603
UMLS CUI [1,2]
C0018246
UMLS CUI [1,3]
C0023216
UMLS CUI [1,4]
C1314939
life expectancy of less than 2 years
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
prior leg bypass on the ipsilateral limb
Description

Bypass Limb Ipsilateral

Data type

boolean

Alias
UMLS CUI [1,1]
C0741847
UMLS CUI [1,2]
C0015385
UMLS CUI [1,3]
C0441989

Similar models

Eligibility Of Bypass Graft of the Extremities NCT02492854

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age > 35 years
boolean
C0001779 (UMLS CUI [1])
Lower Extremity Bypass | Harvest Great saphenous vein Ipsilateral
Item
patient to undergo lower extremity bypass using ipsilateral great saphenous vein harvest
boolean
C0023216 (UMLS CUI [1,1])
C0741847 (UMLS CUI [1,2])
C1512335 (UMLS CUI [2,1])
C1278976 (UMLS CUI [2,2])
C0441989 (UMLS CUI [2,3])
Protocol Compliance | Informed Consent
Item
willing to comply with protocol, attend follow-up appointments, complete all study assessments, and provide written informed consent.
boolean
C0525058 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Investigational New Drugs Peripheral Arterial Disease | Study Subject Participation Status Interventional Study
Item
patients who received an investigational drug for peripheral arterial disease within 4 weeks of screening or who participated in another non-observational clinical trial in the prior 30 days
boolean
C0013230 (UMLS CUI [1,1])
C1704436 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2,1])
C3274035 (UMLS CUI [2,2])
Informed Consent Unable | Informed Consent Refused
Item
inability or refusal to provide informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Immunosuppressive Agents | Chemotherapy | Therapeutic radiology procedure
Item
current immune-suppressive medication, chemotherapy, or radiation therapy
boolean
C0021081 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
C1522449 (UMLS CUI [3])
Revascularization Inguinal Leg Involved
Item
any infrainguinal revascularization procedure on index leg within 12 weeks prior to treatment
boolean
C0581603 (UMLS CUI [1,1])
C0018246 (UMLS CUI [1,2])
C0023216 (UMLS CUI [1,3])
C1314939 (UMLS CUI [1,4])
Life Expectancy
Item
life expectancy of less than 2 years
boolean
C0023671 (UMLS CUI [1])
Bypass Limb Ipsilateral
Item
prior leg bypass on the ipsilateral limb
boolean
C0741847 (UMLS CUI [1,1])
C0015385 (UMLS CUI [1,2])
C0441989 (UMLS CUI [1,3])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

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