ID

31887

Description

Pilot Study of PDL to Treat BCC and SCCIS; ODM derived from: https://clinicaltrials.gov/show/NCT01245972

Link

https://clinicaltrials.gov/show/NCT01245972

Keywords

Versions (1)
  1. 10/7/18 10/7/18 -
Copyright Holder

University of California, San Diego

Uploaded on

October 7, 2018

DOI

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License

Creative Commons BY-NC 3.0
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Eligibility Basal Cell Carcinoma NCT01245972

English

Eligibility Basal Cell Carcinoma NCT01245972

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients requiring surgical excision (conventional or mohs) for biopsy-proven basal cell carcinoma and biopsy-proven squamous cell carcinoma in situ, that is clinically present at the pre-operative visit and measures greater than 0.4cm and less than 3cm in size.
Description

Biopsy confirmed BCC and squamous cell carcinoma requiring surgery

Data type

boolean

Alias
UMLS CUI [1,1]
C0007117
UMLS CUI [1,2]
C0449575
UMLS CUI [1,3]
C1514873
UMLS CUI [1,4]
C0728940
UMLS CUI [2,1]
C0007137
UMLS CUI [2,2]
C0007099
UMLS CUI [2,3]
C0449575
UMLS CUI [2,4]
C1514873
UMLS CUI [2,5]
C0728940
UMLS CUI [3]
C0449453
lesions in the trunk, extremities, and scalp
Description

Lesions in trunk, extremities and scalp

Data type

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0460005
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C0015385
UMLS CUI [3,1]
C0221198
UMLS CUI [3,2]
C0036270
presence of clinically identifiable residual tumor.
Description

Residual tumor

Data type

boolean

Alias
UMLS CUI [1,1]
C0543478
UMLS CUI [1,2]
C0205210
patients, males and females, aged 18-90 years.
Description

Gender and Age

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
willing to participate.
Description

Willing to participate

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C0600109
able to give informed consent.
Description

Ability for Informed consent

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0085732
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age younger than 18 years
Description

Child

Data type

boolean

Alias
UMLS CUI [1,1]
C0008059
UMLS CUI [1,2]
C0001779
location of lesion not in the trunk, extremities, and scalp
Description

Lesion location not in trunk, extremity and scalp

Data type

boolean

Alias
UMLS CUI [1,1]
C0221198
UMLS CUI [1,2]
C0460005
UMLS CUI [1,3]
C1272460
UMLS CUI [2,1]
C0221198
UMLS CUI [2,2]
C0015385
UMLS CUI [2,3]
C1272460
UMLS CUI [3,1]
C0221198
UMLS CUI [3,2]
C0036270
UMLS CUI [3,3]
C1272460
fitzpatrick skin type v or vi.
Description

Fitzpatrick skin type

Data type

boolean

Alias
UMLS CUI [1]
C2732923
prior history of known light sensitivity.
Description

Photosensitivity

Data type

boolean

Alias
UMLS CUI [1]
C0349506
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
cognitive impairment
Description

Cognitive impairment

Data type

boolean

Alias
UMLS CUI [1]
C0338656
prisoner
Description

Prisoner

Data type

boolean

Alias
UMLS CUI [1]
C0033167
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Similar models

Eligibility Basal Cell Carcinoma NCT01245972

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Biopsy confirmed BCC and squamous cell carcinoma requiring surgery
Item
patients requiring surgical excision (conventional or mohs) for biopsy-proven basal cell carcinoma and biopsy-proven squamous cell carcinoma in situ, that is clinically present at the pre-operative visit and measures greater than 0.4cm and less than 3cm in size.
boolean
C0007117 (UMLS CUI [1,1])
C0449575 (UMLS CUI [1,2])
C1514873 (UMLS CUI [1,3])
C0728940 (UMLS CUI [1,4])
C0007137 (UMLS CUI [2,1])
C0007099 (UMLS CUI [2,2])
C0449575 (UMLS CUI [2,3])
C1514873 (UMLS CUI [2,4])
C0728940 (UMLS CUI [2,5])
C0449453 (UMLS CUI [3])
Lesions in trunk, extremities and scalp
Item
lesions in the trunk, extremities, and scalp
boolean
C0221198 (UMLS CUI [1,1])
C0460005 (UMLS CUI [1,2])
C0221198 (UMLS CUI [2,1])
C0015385 (UMLS CUI [2,2])
C0221198 (UMLS CUI [3,1])
C0036270 (UMLS CUI [3,2])
Residual tumor
Item
presence of clinically identifiable residual tumor.
boolean
C0543478 (UMLS CUI [1,1])
C0205210 (UMLS CUI [1,2])
Gender and Age
Item
patients, males and females, aged 18-90 years.
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Willing to participate
Item
willing to participate.
boolean
C2348568 (UMLS CUI [1,1])
C0600109 (UMLS CUI [1,2])
Ability for Informed consent
Item
able to give informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Child
Item
age younger than 18 years
boolean
C0008059 (UMLS CUI [1,1])
C0001779 (UMLS CUI [1,2])
Lesion location not in trunk, extremity and scalp
Item
location of lesion not in the trunk, extremities, and scalp
boolean
C0221198 (UMLS CUI [1,1])
C0460005 (UMLS CUI [1,2])
C1272460 (UMLS CUI [1,3])
C0221198 (UMLS CUI [2,1])
C0015385 (UMLS CUI [2,2])
C1272460 (UMLS CUI [2,3])
C0221198 (UMLS CUI [3,1])
C0036270 (UMLS CUI [3,2])
C1272460 (UMLS CUI [3,3])
Fitzpatrick skin type
Item
fitzpatrick skin type v or vi.
boolean
C2732923 (UMLS CUI [1])
Photosensitivity
Item
prior history of known light sensitivity.
boolean
C0349506 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Cognitive impairment
Item
cognitive impairment
boolean
C0338656 (UMLS CUI [1])
Prisoner
Item
prisoner
boolean
C0033167 (UMLS CUI [1])
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