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Informations:
Erreur:
ID
26570
Description
Coated VICRYL* Plus Suture Compared to Chinese Silk in Scheduled Breast Cancer Surgery; ODM derived from: https://clinicaltrials.gov/show/NCT00768222
Lien
https://clinicaltrials.gov/show/NCT00768222
Mots-clés
Versions (2)
- 19/10/2017 19/10/2017 -
- 22/10/2017 22/10/2017 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
19 octobre 2017
DOI
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Licence
Creative Commons BY-NC 3.0
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Eligibility Breast Cancer NCT00768222
Eligibility Breast Cancer NCT00768222
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT00768222
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Age | Informed Consent
Item
18 years of age or older with written informed consent
boolean
C0001779 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
C0021430 (UMLS CUI [2])
Modified radical mastectomy Scheduled
Item
scheduled for a modified radical mastectomy
boolean
C0024883 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,2])
Surgical wound Surgical wound classification
Item
surgical wound classified class i/clean using the cdc ssi surgical wound classification
boolean
C0332803 (UMLS CUI [1,1])
C2038494 (UMLS CUI [1,2])
C2038494 (UMLS CUI [1,2])
Informed Consent Unable | Protocol Compliance Unlikely | Follow-up visit Completion Unlikely
Item
unable to give consent and unlikely to comply with study requirements and complete the 90-day follow up visit
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
C0589121 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C0750558 (UMLS CUI [3,3])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C0750558 (UMLS CUI [2,2])
C0589121 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C0750558 (UMLS CUI [3,3])
Operative Surgical Procedures | Modified radical mastectomy | Mammaplasty Immediate | Breast cosmetic surgery | Cosmetic breast reduction | Cosmetic breast augmentation | Breast implant procedure | Mammary duct ectasia | Communicable Disease Breast | Infection of breast implant
Item
undergoing surgery for modified radical mastectomy with immediate breast reconstruction, cosmetic breast operations, reduction, expansion, insertion of prothesis, duct ectasia or infective breast disease or implant
boolean
C0543467 (UMLS CUI [1])
C0024883 (UMLS CUI [2])
C0085076 (UMLS CUI [3,1])
C0205253 (UMLS CUI [3,2])
C0549358 (UMLS CUI [4])
C1390445 (UMLS CUI [5])
C1390444 (UMLS CUI [6])
C0178391 (UMLS CUI [7])
C0152442 (UMLS CUI [8])
C0009450 (UMLS CUI [9,1])
C0006141 (UMLS CUI [9,2])
C0405488 (UMLS CUI [10])
C0024883 (UMLS CUI [2])
C0085076 (UMLS CUI [3,1])
C0205253 (UMLS CUI [3,2])
C0549358 (UMLS CUI [4])
C1390445 (UMLS CUI [5])
C1390444 (UMLS CUI [6])
C0178391 (UMLS CUI [7])
C0152442 (UMLS CUI [8])
C0009450 (UMLS CUI [9,1])
C0006141 (UMLS CUI [9,2])
C0405488 (UMLS CUI [10])
Surgical wound Surgical wound classification
Item
surgical wounds classified as class ii, iii or iv using cdc ssi surgical wound classification
boolean
C0332803 (UMLS CUI [1,1])
C2038494 (UMLS CUI [1,2])
C2038494 (UMLS CUI [1,2])
Malignant Neoplasms inflammatory | Skin Ulcer inflammatory
Item
has inflammatory cancers or skin ulceration
boolean
C0006826 (UMLS CUI [1,1])
C0333348 (UMLS CUI [1,2])
C0037299 (UMLS CUI [2,1])
C0333348 (UMLS CUI [2,2])
C0333348 (UMLS CUI [1,2])
C0037299 (UMLS CUI [2,1])
C0333348 (UMLS CUI [2,2])
Triclosan allergy | Intolerance to Triclosan
Item
has known allergy or intolerance to triclosan
boolean
C0571330 (UMLS CUI [1])
C1744706 (UMLS CUI [2,1])
C0040958 (UMLS CUI [2,2])
C1744706 (UMLS CUI [2,1])
C0040958 (UMLS CUI [2,2])
Impaired wound healing | Immunologic Deficiency Syndromes chronic | Diabetes Mellitus | Steroid use Prolonged | AIDS | Substance Use Disorders
Item
has compromised wound healing or chronic immune deficiency, for example diabetes, prolonged steroid use, aids or substance abuse
boolean
C0151692 (UMLS CUI [1])
C0021051 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0011849 (UMLS CUI [3])
C0281991 (UMLS CUI [4,1])
C0439590 (UMLS CUI [4,2])
C0001175 (UMLS CUI [5])
C0038586 (UMLS CUI [6])
C0021051 (UMLS CUI [2,1])
C0205191 (UMLS CUI [2,2])
C0011849 (UMLS CUI [3])
C0281991 (UMLS CUI [4,1])
C0439590 (UMLS CUI [4,2])
C0001175 (UMLS CUI [5])
C0038586 (UMLS CUI [6])
Heart Disease Serious | Lung disease Serious
Item
has serious heart and/or lung disease
boolean
C0018799 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0024115 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C0205404 (UMLS CUI [1,2])
C0024115 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
Skin Scar | Skin Scar Family history
Item
has skin scar history or family history
boolean
C0241158 (UMLS CUI [1])
C0241158 (UMLS CUI [2,1])
C0241889 (UMLS CUI [2,2])
C0241158 (UMLS CUI [2,1])
C0241889 (UMLS CUI [2,2])
Study Subject Participation Status | Relationship Clinical Trial | Involvement with Clinical Trial
Item
has direct relationship to or involvement in this or other studies under the direction of the investigator or center
boolean
C2348568 (UMLS CUI [1])
C0439849 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C1314939 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
C0439849 (UMLS CUI [2,1])
C0008976 (UMLS CUI [2,2])
C1314939 (UMLS CUI [3,1])
C0008976 (UMLS CUI [3,2])
Investigational New Drugs | Investigational Medical Device
Item
received an experimental drug or device within 30 days prior to the planned start of treatment
boolean
C0013230 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C2346570 (UMLS CUI [2])