ID

23429

Beskrivning

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

Länk

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

Nyckelord

Versioner (1)
  1. 2017-07-04 2017-07-04 -
Uppladdad den

4 juli 2017

DOI

För en begäran logga in.

Licens

Creative Commons BY 4.0
Modellkommentarer :

Här kan du kommentera modellen. Med hjälp av pratbubblor i Item-grupperna och Item kan du lägga in specifika kommentarer.

Tillbaka till modellkommentarer
Itemgroup-kommentar för :

Item-kommentar för :

Du måste vara inloggad för att kunna ladda ner formulär. Var vänlig logga in eller registrera dig utan kostnad.

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

Engelsk

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

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

Age

Datatyp

boolean

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

Wound-healing

Datatyp

boolean

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

Wound Diameter

Datatyp

boolean

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

Wound surface

Datatyp

boolean

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

Exclusion Criteria

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

Infrastructure

Datatyp

boolean

Alias
UMLS CUI [1]
C1998546
Healthy Volunteers
Beskrivning

Control Group

Datatyp

boolean

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

Open abdominal fascia

Datatyp

boolean

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

Organ failure

Datatyp

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
Beskrivning

Start of Vacuum Device

Datatyp

boolean

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

Ongoing after chemotherapy

Datatyp

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
Beskrivning

Ongoing after radiotherapy

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0549178
UMLS CUI [1,2]
C1522449
Tillbaka till toppen

Similar models

Eligibility Wound Therapy After Surgery NCT01611207 DRKS ID 00003498

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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])
Tillbaka till toppen 

Kontakt

Använd detta formulär för feedback, frågor och förslag på förbättringar.

Fält markerade med * är obligatoriska.

Hjälp

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