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NCT01454167 Clinical Trial

Acid Base and Electrolytes Patterns in Drains Operational Wounds and Its Relation to Complications

Infections Clinical Trial

Official title:
Acid Base and Electrolytes Patterns in Drains of Different Operational Wounds and Its Relation to Specific Infections and Seroma Formation

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01454167
Other study ID # CMC-13-0130-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received October 14, 2011
Last updated May 25, 2015
Start date May 2014
Est. completion date April 2016

Study information
Verified date May 2015
Source Carmel Medical Center
Contact Nir Gal Or, Dr
Phone 0545454636
Email nirgalor@gmail.com
Is FDA regulated No
Health authority Israel: Ethics Commission
Study type Observational

Clinical Trial Summary

Objective- The purpose of this study is to evaluate a connection between PH,PCO2,HCO3,PO2,Na,K,Glu and Lactate patterns in vacuum drains of different plastic operational wounds and its relation to infections and seroma formation.

Description:

our objective is evaluation of a connection between PH,PCO2,HCO3,PO2,Na,K,Glu and Lactate patterns in vacum drains of different plastic operational wounds and its relation to infections and seroma formation.

it is possible that early changes in this values might point out an infection or seroma formation of a wound before clinical signs appear.

Recruitment information / eligibility
Status Recruiting
Enrollment 200
Est. completion date April 2016
Est. primary completion date April 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- all post operational patients who have a vacum drain/s

Exclusion Criteria:

- patients who are unable to sign a Consent Form (demented,Alzheimer's disease ...)

- patients who refuse participation

Study Design

Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Israel Carmel Medical Center Haifa

Sponsors (1)
Lead Sponsor Collaborator
Carmel Medical Center

Country where clinical trial is conducted

Israel, 

Outcome
Type Measure Description Time frame Safety issue
Primary Histological confirmation end of treatment No
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