NCT00765141

Brief 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.

Trial Health

30
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Timeline
Completed

Started Jun 2008

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
withdrawn

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

June 1, 2008

Completed
4 months until next milestone

First Submitted

Initial submission to the registry

September 30, 2008

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 2, 2008

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2009

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2009

Completed
Last Updated

November 26, 2015

Status Verified

November 1, 2015

Enrollment Period

9 months

First QC Date

September 30, 2008

Last Update Submit

November 24, 2015

Conditions

Infection

Keywords

wound debridementremoved orthopedic implantsremoved catheters or shuntsexcised tonsilsamputated tissuesputum, stoolor other excretions.

Study Arms (1)

No treatment

Eligibility Criteria

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

The samples can include material such as wound debridement, removed orthopedic implants, removed catheters or shunts, excised tonsils, amputated tissue, sputum, stool, or other excretions.

You may qualify if:

  • The Subject must be 18 years of age or older.
  • The Subject must be mentally competent as determined by the Investigator.

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Southwest Regional Wound Care Center

Lubbock, Texas, 79410, United States

Location

Biospecimen

Retention: SAMPLES WITH DNA

The samples can include material such as wound debridement, removed orthopedic implants, removed catheters or shunts, excised tonsils, amputated tissue, sputum, stool, or other excretions.

MeSH Terms

Conditions

Infections

Study Officials

  • Randall Wolcott, MD

    Southwest Regional Wound Care Center

    PRINCIPAL INVESTIGATOR
0

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

September 30, 2008

First Posted

October 2, 2008

Study Start

June 1, 2008

Primary Completion

March 1, 2009

Study Completion

March 1, 2009

Last Updated

November 26, 2015

Record last verified: 2015-11

Locations

US(1)