Eligibility Diabetic Foot Wounds NCT01480362 DRKS00003347

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Presence of diabetes mellitus
Beskrivning

Diabetes Mellitus

Datatyp

boolean

Alias
UMLS CUI [1]
C0011849
Presence of a foot wound (chronic wounds; amputation wounds) Wagner stage 2-4
Beskrivning

Wagner Stage

Datatyp

boolean

Alias
UMLS CUI [1]
C0149697
Existence of the foot wound for at least 4 weeks
Beskrivning

Foot Wound: Length

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0149697
UMLS CUI [1,2]
C0872146
Signed informed consent form
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
Patient's eligibility of NPWT in the opinion of the treating physician
Beskrivning

Negative Pressure Wound Therapy

Datatyp

boolean

Alias
UMLS CUI [1]
C1956078
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Beskrivning

Control Group

Datatyp

boolean

Alias
UMLS CUI [1]
C0009932
Age <18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
Non-Compliance
Beskrivning

Compliance

Datatyp

boolean

Alias
UMLS CUI [1]
C1321605
Pregnancy
Beskrivning

Pregnancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
Allergies regarding the release of substances from components of each treatment arm
Beskrivning

Hypersensitivity to Study Drug

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0304229
Severe anemia, wich was not caused by an infection
Beskrivning

Anemia

Datatyp

boolean

Alias
UMLS CUI [1]
C0002871
Simultaneous participation of patients in another interventional study / previous participation in the same study
Beskrivning

Study Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
Use of NPWT systems to the study-related foot lesion within a period of 6 weeks prior to study inclusion
Beskrivning

Previous Negative Pressure Wound Therapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C1956078
Presence of necrotic tissue with eschar, which can not be removed
Beskrivning

Necrotic tissue

Datatyp

boolean

Alias
UMLS CUI [1]
C2321738
Untreated osteitis or osteomyelitis
Beskrivning

Osteitis or osteomyelitis

Datatyp

boolean

Alias
UMLS CUI [1]
C0029400
UMLS CUI [2]
C0029443
Not examined / unexplored fistula
Beskrivning

Fistula

Datatyp

boolean

Alias
UMLS CUI [1]
C0016169
Malignancy of the wound
Beskrivning

Malignancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0006826
Exposed: nerves, blood vessels, anastomotic site
Beskrivning

Site of Lesion

Datatyp

boolean

Alias
UMLS CUI [1]
C0449695
ambulant NPWT of patients receiving anticoagulants (especially heparinization or marcumar therapy) or with otherwise highly impaired clotting function, which have a risk of circulatory relevant bleeding
Beskrivning

Bleeding Risk

Datatyp

boolean

Alias
UMLS CUI [1]
C3251812

Similar models

Eligibility Diabetic Foot Wounds NCT01480362 DRKS00003347

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Diabetes Mellitus
Item
Presence of diabetes mellitus
boolean
C0011849 (UMLS CUI [1])
Wagner Stage
Item
Presence of a foot wound (chronic wounds; amputation wounds) Wagner stage 2-4
boolean
C0149697 (UMLS CUI [1])
Foot Wound: Length
Item
Existence of the foot wound for at least 4 weeks
boolean
C0149697 (UMLS CUI [1,1])
C0872146 (UMLS CUI [1,2])
Informed Consent
Item
Signed informed consent form
boolean
C0021430 (UMLS CUI [1])
Negative Pressure Wound Therapy
Item
Patient's eligibility of NPWT in the opinion of the treating physician
boolean
C1956078 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Age
Item
Age <18 years
boolean
C0001779 (UMLS CUI [1])
Compliance
Item
Non-Compliance
boolean
C1321605 (UMLS CUI [1])
Pregnancy
Item
Pregnancy
boolean
C0032961 (UMLS CUI [1])
Hypersensitivity to Study Drug
Item
Allergies regarding the release of substances from components of each treatment arm
boolean
C0020517 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
Anemia
Item
Severe anemia, wich was not caused by an infection
boolean
C0002871 (UMLS CUI [1])
Study Participation Status
Item
Simultaneous participation of patients in another interventional study / previous participation in the same study
boolean
C2348568 (UMLS CUI [1])
Previous Negative Pressure Wound Therapy
Item
Use of NPWT systems to the study-related foot lesion within a period of 6 weeks prior to study inclusion
boolean
C0205156 (UMLS CUI [1,1])
C1956078 (UMLS CUI [1,2])
Necrotic tissue
Item
Presence of necrotic tissue with eschar, which can not be removed
boolean
C2321738 (UMLS CUI [1])
Osteitis or osteomyelitis
Item
Untreated osteitis or osteomyelitis
boolean
C0029400 (UMLS CUI [1])
C0029443 (UMLS CUI [2])
Fistula
Item
Not examined / unexplored fistula
boolean
C0016169 (UMLS CUI [1])
Malignancy
Item
Malignancy of the wound
boolean
C0006826 (UMLS CUI [1])
Site of Lesion
Item
Exposed: nerves, blood vessels, anastomotic site
boolean
C0449695 (UMLS CUI [1])
Bleeding Risk
Item
ambulant NPWT of patients receiving anticoagulants (especially heparinization or marcumar therapy) or with otherwise highly impaired clotting function, which have a risk of circulatory relevant bleeding
boolean
C3251812 (UMLS CUI [1])