ID

23429

Description

Responsible Party: Dr. Marcus Redaèlli, Administative and scientific head of staffed offices of Interdisciplinary Centre for Health Services Research, University of Witten/Herdecke ClinicalTrials.gov Identifier: NCT01611207 History of Changes Other Study ID Numbers: 03-2012 DRKS ID 00003498 ( Registry Identifier: German Clinical Trials Register ) Study First Received: March 28, 2012 Last Updated: May 17, 2013 Evaluate the Efficacy of the Treatment of Iatrogenic Subcutaneous Abdominal Wounds (ISAW) After Surgery by Application of Negative Pressure Wound Therapy (NPWT) in Comparison to Standard Conventional Wound Therapy (SCWT) of the Clinical Routine (ISAW) ODM derived from: https://clinicaltrials.gov/ct2/show/NCT01611207

Link

https://clinicaltrials.gov/ct2/show/NCT01611207

Keywords

Versions (1)
  1. 7/4/17 7/4/17 -
Uploaded on

July 4, 2017

DOI

To request one please log in.

License

Creative Commons BY 4.0
Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Back to model comments
Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

English

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Ages Eligible for Study: 18 Years and older (Adult, Senior)
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Acute subcutaneous abdominal wound-healing impairment after surgical intervention
Description

Wound-healing

Data type

boolean

Alias
UMLS CUI [1]
C0043240
Sizes of wound opening (maximum diameter ≥ 3 cm)
Description

Wound Diameter

Data type

boolean

Alias
UMLS CUI [1,1]
C0043250
UMLS CUI [1,2]
C1301886
Wound surface ≥ 9 qcm
Description

Wound surface

Data type

boolean

Alias
UMLS CUI [1,1]
C0043250
UMLS CUI [1,2]
C0205148
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Lack of infrastructure for outpatient continuation of treatment and study-specific interventions
Description

Infrastructure

Data type

boolean

Alias
UMLS CUI [1]
C1998546
Healthy Volunteers
Description

Control Group

Data type

boolean

Alias
UMLS CUI [1]
C0009932
Existence of an open abdominal fascia
Description

Open abdominal fascia

Data type

boolean

Alias
UMLS CUI [1,1]
C0225222
UMLS CUI [1,2]
C0332798
Acute serious organ failure
Description

Organ failure

Data type

boolean

Alias
UMLS CUI [1]
C0231174
Application of an other active vacuum device at the wound treated during the study conduct within 8 days before screening visit
Description

Start of Vacuum Device

Data type

boolean

Alias
UMLS CUI [1,1]
C1690010
UMLS CUI [1,2]
C0439659
Ongoing / during 3 weeks after chemo therapy
Description

Ongoing after chemotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C0392920
Ongoing / during 3 weeks after radiation therapy Contraindications in accordance with the safety precautions issued by the FDA or the companies
Description

Ongoing after radiotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C1522449
Back to the top of the page

Similar models

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
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])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
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])
Back to the top of the page 

Contact

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Help

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial