Prevention of Bacteremia Induced by Debridement of Pressure Ulcer

This study has been terminated.
Sponsor:
Information provided by:
Herzog Hospital
ClinicalTrials.gov Identifier:
NCT00269100
First received: December 22, 2005
Last updated: April 19, 2007
Last verified: April 2007
  Purpose

The purpose of this study is to analyse bacteremia induced by debridement of pressure ulcers in patients in the complex nursing department.


Condition Phase
Pressure Ulcers
Bacteremia
Phase 1
Phase 2

Study Type: Observational
Study Design: Observational Model: Defined Population
Primary Purpose: Screening
Time Perspective: Longitudinal
Time Perspective: Prospective

Resource links provided by NLM:


Further study details as provided by Herzog Hospital:

Estimated Enrollment: 60
  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patient in the complex nursing department
  • With contaminated pressure ulcers
  • Going to have a debridement procedure

Exclusion Criteria:

  • Penicillin sensitivity
  • Bacteremia that does not react to the antibiotic treatment
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00269100

Locations
Israel
Herzog Hospital
Jerusalem, Israel, 91351
Sponsors and Collaborators
Herzog Hospital
Investigators
Study Director: Efraim Jaul Herzog Hospital
  More Information

No publications provided

ClinicalTrials.gov Identifier: NCT00269100     History of Changes
Other Study ID Numbers: Jaul1CTIL
Study First Received: December 22, 2005
Last Updated: April 19, 2007
Health Authority: Israel: Israeli Health Ministry Pharmaceutical Administration

Keywords provided by Herzog Hospital:
Debridement

Additional relevant MeSH terms:
Bacteremia
Pressure Ulcer
Ulcer
Bacterial Infections
Sepsis
Infection
Systemic Inflammatory Response Syndrome
Inflammation
Pathologic Processes
Skin Ulcer
Skin Diseases

ClinicalTrials.gov processed this record on October 16, 2012