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Swab Sample Collection for the Detection of Bacterial Proteases in Wounds Assay

Swab Sample Collection for the Detection of Bacterial Proteases in Wounds Assay

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01750203
Enrollment
135
Registered
2012-12-17
Start date
2012-12-31
Completion date
2012-12-31
Last updated
2012-12-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Wounds With Different Etiologies

Keywords

Diabetic foot ulcers, venous leg ulcers, pressure sores, acute wounds

Brief summary

The objective of this study is to collect wound exudate (fluid) swab samples from Subjects who have wounds that show clinical signs of infection, as well as from Subjects who have wounds that do not show clinical signs of infection. Swab samples will be collected from acute and chronic wounds of different etiologies and these will be analysed for bacteria types and markers of infection.

Interventions

OTHERSwabs

There is no intervention only swabs are being used to collect wound fluid samples

Sponsors

Systagenix Wound Management
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Subject has presented to participating study site with a wound(s) suspected to be infected, as determined by the Investigator and/ or study staff - defined as one that through clinical judgment has questionable infection status, and /or shows three or more of the NERDS or STONES signs of infection); * Subject has presented to participating study site with a wound(s) suspected not to be infected, as determined by the Investigator and/ or study staff - defined as one that does not show three or more of the NERDS or STONES signs of infection. * Subject is 18 years of age or older. * Subject agrees to complete all aspects of the study and provides Informed Consent

Exclusion criteria

* Subject is less than 18 years of age. * Target wound contains a malignancy * Subject has hypersensitivity of the wound or painful wound surface which prevents touching/swabbing of the wound surface. * Subject is confirmed to be positive for HIV or hepatitis. * Subject is unable or unwilling to provide informed consent. * Subjects deemed inappropriate for the study by the site's Principal Investigator.

Design outcomes

Primary

MeasureTime frameDescription
The biochemical differences between clinically infected and non infected wounds.1 dayWound exudate (fluid) swab samples from different etiologies of wounds will be collected. Subjects who have wounds that do not show clinical signs of infection, as well as Subjects who have wounds that do show clinical signs of infection will be enrolled. a maximum of four (4) swab sample from Subjects from whom Informed Consent has been obtained. The swabs will be subjected to various tests methods that may include, but are not limited to, the following: 1) quantitative bacterial cultures (for aerobic and / or anaerobic bacteria), 2) for research use only testing on test formats currently in development by the sponsor (note: this data will not be used to support regulatory filings, such as CE marking or FDA submissions for U.S. market clearance), 3) molecular microbiology, and 4) protease analysis.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026