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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03386175
Other study ID # 38RC17.054
Secondary ID 2017-A00742-51
Status Recruiting
Phase
First received
Last updated
Start date October 4, 2017
Est. completion date December 3, 2020

Study information

Verified date August 2020
Source University Hospital, Grenoble
Contact sophie blaise, MD PhD
Phone 0033476765547
Email SBlaise@chu-grenoble.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

the aim of the study is to evaluate the efficiency of the therapy with negative pression (TPN) and instillation in the debridement of chronic wound


Description:

it is an observation study with only the aim to evaluate the percentage of fibrin before and after the specific treatment of TPN


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 3, 2020
Est. primary completion date December 3, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- wound with debridement

Exclusion Criteria:

-

Study Design


Related Conditions & MeSH terms


Intervention

Device:
therapy with negative pression and instillation
therapy with negative pression and instillation

Locations

Country Name City State
France Grenoble University hospital Grenoble

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary percentage of fibrine percentage of fibrine 1 day
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