NCT00794742

Brief Summary

The purpose of this study is to test the resistance of pathogenic bacteria in infected tissues of burn patients to various antimicrobials and enzyme debriders.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
32

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Nov 2008

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Study Start

First participant enrolled

November 1, 2008

Completed
18 days until next milestone

First Submitted

Initial submission to the registry

November 19, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 20, 2008

Completed
5.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2014

Completed
Last Updated

April 13, 2015

Status Verified

April 1, 2015

Enrollment Period

5.5 years

First QC Date

November 19, 2008

Last Update Submit

April 9, 2015

Conditions

Burns

Keywords

BurnAntimicrobialBacteriaResistanceBiofilmPathogen

Outcome Measures

Primary Outcomes (1)

  • Types of bacteria

    28 days

Study Arms (1)

Burn Wounds

Patients with burn wounds

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Patients with open,unhealed,burn wounds

You may qualify if:

  • Males and females of any age
  • Have open, unhealed wounds(s) that will be cultured per standard of care
  • Subject or authorized representative provide informed consent

You may not qualify if:

  • Informed consent not provided or able to be obtained

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University Medical Center

Lubbock, Texas, 79415, United States

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Bacterial isolates of infected burn wounds

MeSH Terms

Conditions

Burns

Condition Hierarchy (Ancestors)

Wounds and Injuries

Study Officials

  • John Griswold, M.D.

    Texas Tech University Health Sciences Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 19, 2008

First Posted

November 20, 2008

Study Start

November 1, 2008

Primary Completion

May 1, 2014

Study Completion

May 1, 2014

Last Updated

April 13, 2015

Record last verified: 2015-04

Locations

US(1)