Age
Item
Ages Eligible for Study: 18 Years and older (Adult, Senior)
boolean
C0001779 (UMLS CUI [1])
Wound-healing
Item
Acute subcutaneous abdominal wound-healing impairment after surgical intervention
boolean
C0043240 (UMLS CUI [1])
Wound Diameter
Item
Sizes of wound opening (maximum diameter ≥ 3 cm)
boolean
C0043250 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
Wound surface
Item
Wound surface ≥ 9 qcm
boolean
C0043250 (UMLS CUI [1,1])
C0205148 (UMLS CUI [1,2])
Infrastructure
Item
Lack of infrastructure for outpatient continuation of treatment and study-specific interventions
boolean
C1998546 (UMLS CUI [1])
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
Open abdominal fascia
Item
Existence of an open abdominal fascia
boolean
C0225222 (UMLS CUI [1,1])
C0332798 (UMLS CUI [1,2])
Organ failure
Item
Acute serious organ failure
boolean
C0231174 (UMLS CUI [1])
Start of Vacuum Device
Item
Application of an other active vacuum device at the wound treated during the study conduct within 8 days before screening visit
boolean
C1690010 (UMLS CUI [1,1])
C0439659 (UMLS CUI [1,2])
Ongoing after chemotherapy
Item
Ongoing / during 3 weeks after chemo therapy
boolean
C0549178 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
Ongoing after radiotherapy
Item
Ongoing / during 3 weeks after radiation therapy Contraindications in accordance with the safety precautions issued by the FDA or the companies
boolean
C0549178 (UMLS CUI [1,1])
C1522449 (UMLS CUI [1,2])