ID

36697

Description

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

Lien

https://clinicaltrials.gov/show/NCT02492854

Mots-clés

  1. 02.06.19 02.06.19 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

2. Juni 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

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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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

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

Type de données

boolean

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

Bypass Limb Ipsilateral

Type de données

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)
Type de données
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])

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