A Multi-Center Protocol for Obtaining and Storing Human Samples for Immediate or Future Microbial, Immune, or Host Microbe Scientific Study

Infection Clinical Trial

Official title:

A Multi-Center Protocol for Obtaining and Storing Human Samples for Immediate or Future Microbial, Immune, or Host Microbe Scientific Study

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00765141
• Other study ID #: 56-RW-011
• Status: Withdrawn
• Phase: N/A
• First received: September 30, 2008
• Last updated: November 24, 2015
• Start date: June 2008
• Est. completion date: March 2009

Study information

• Verified date: November 2015
• Source: Southwest Regional Wound Care Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

The intent of this protocol is to salvage human-related material that is normally destined for destruction, so it can be used in infection-related scientific studies.

Description:

This clinical material can be studied in order to better understand the molecular, cellular, or ecological components of the infected or potentially infected tissue or device. These studies may be able to provide important insights into the keys of chronic infections, complex infections, medical biofilms, pathogen ecology, and healing.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: March 2009
• Est. primary completion date: March 2009
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• The Subject must be 18 years of age or older.

• The Subject must be mentally competent as determined by the Investigator.

Exclusion Criteria:

• The Subject may not be currently incarcerated.

• The Subject may not be knowingly pregnant.

• The Subject may not be institutionalized.

• The Subject may not be an employee or student of the investigator or sponsor.

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Infection

Locations

Country	Name	City	State
United States	Southwest Regional Wound Care Center	Lubbock	Texas

Sponsors (1)

Lead Sponsor	Collaborator
Southwest Regional Wound Care Center

Country where clinical trial is conducted

United States,