NCT01454167

Brief 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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
200

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started May 2014

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 14, 2011

Completed
4 days until next milestone

First Posted

Study publicly available on registry

October 18, 2011

Completed
2.5 years until next milestone

Study Start

First participant enrolled

May 1, 2014

Completed
1.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2016

Completed
Last Updated

May 27, 2015

Status Verified

May 1, 2015

Enrollment Period

1.9 years

First QC Date

October 14, 2011

Last Update Submit

May 25, 2015

Conditions

WoundsInfectionsSeroma

Keywords

vacum drainsoperational woundsinfectionsseromaacid baseglucoselactate

Outcome Measures

Primary Outcomes (1)

  • Histological confirmation

    end of treatment

Eligibility Criteria

Age18 Years - 90 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

all post operational patients who have a vacuum drain/s

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Carmel Medical Center

Haifa, Israel

RECRUITING

MeSH Terms

Conditions

Wounds and InjuriesInfectionsSeroma

Condition Hierarchy (Ancestors)

InflammationPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Nir Gal Or, Dr

    carmel medical center- ISRAEL

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nir Gal Or, Dr

CONTACT

0545454636nirgalor@gmail.com

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
professor

Study Record Dates

First Submitted

October 14, 2011

First Posted

October 18, 2011

Study Start

May 1, 2014

Primary Completion

April 1, 2016

Study Completion

April 1, 2016

Last Updated

May 27, 2015

Record last verified: 2015-05

Locations

IL(1)