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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03905213
Other study ID # MICRO.HGUGM.2018-008
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date September 1, 2019
Est. completion date August 28, 2021

Study information

Verified date March 2019
Source Hospital General Universitario Gregorio Marañon
Contact Maria Jesus Perez Granda, PhD
Phone +34618355299
Email massus@hotmail.es
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To compare cost effectiveness of a polyurethane dressing or a vacuum therapy dressing versus the conventional gauze in the prevention of superficial wound infection y major cardiac surgery


Description:

It is a clinical prospective and randomized study. patientes will be randomized to three groups on the day of surgery: conventional gauze, polyurethane or vacuum therapy dressing. Clinical al microbiological data will be monitorized to evaluate the infection rate of surgical wound , mediastinitis, days of hospital stay and consumption of antimicrobials.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 900
Est. completion date August 28, 2021
Est. primary completion date August 28, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- patient scheduled to cardiac surgery.

- signed informed consent form

Exclusion Criteria:

- hypersensibility to dressings

Study Design


Intervention

Device:
dressing MEPORE
assignation to three different authorised and on label dressing: conventional dressing (MEPORE)
dressing MEPILEX
assignation to three different authorised and on label dressing: absorbent(MEPILEX)
dressing PICCO
assignation to three different authorised and on label dressing:vacuum Therapy dressing(PICCO)

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Maria Jesus Perez Instituto de Salud Carlos III

Outcome

Type Measure Description Time frame Safety issue
Primary prevention of surgical wound infection surgical wound infection measured as number of patients suffering surgical wound infection during the study period surgery date up to 6 months
Secondary hospital stay days at hospital from hospitalization until an average of 1 year
Secondary antimicrobial consumption defined dose of antimicrobial agents during hospital stay from surgery date until an average of 1 year
Secondary dressing consumption cost number of dressing and its cost from surgery date until an average of 8 weeks
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