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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02981550
Other study ID # Pro18602
Secondary ID
Status Withdrawn
Phase N/A
First received November 30, 2016
Last updated November 7, 2017
Start date November 2016
Est. completion date November 2018

Study information

Verified date November 2017
Source BreathTec Biomedical Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this feasibility study is to test a device which analyzes breath and may allow doctors and health professionals to immediately determine if an ill patient has a specific type of bacterial infection. This will allow a health professional to provide immediate targeted antibiotics to properly start treatment without delay.


Description:

Community acquired, or hospital acquired [nosocomial] infections [pathogens] are a common cause for morbidity and mortality. Initiation of antibiotic treatment is by best guess or using a broad spectrum antibiotic. The improper administration of antibiotics is known to lead to the developing specter of antibiotic resistant organisms.

Certain community acquired bacterial infection such as Streptococcus upper respiratory tract infections carry increased risk of morbidity secondary to risk of developing abscess, glomerulonephritis, and/or rheumatic fever. Commonly, most upper respiratory tract infections are caused by viruses. However due to the unknown pathogen causing an upper respiratory tract infection, with the risks of potential chronic severe complications from Streptococcus, initial treatment starts with either an antibiotic, or a typical 3day wait for bacterial culture result. Quite often, the wait-and-see approach in the community is not undertaken because of the difficulty in returning for a follow-up appointment.

The risk of a developing antibiotic resistant bacteria is well-known and is one of the greatest health threats worldwide leading to longer hospitalizations, higher medical costs and death, according to the World Health Organization. Thus a point of care device which would enable physicians or other medical practitioners to promptly discriminate between Streptococcal or other antibiotic sensitive pathogens versus non antibiotic sensitive viral causes of specific upper respiratory tract infectious pathogens is needed.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date November 2018
Est. primary completion date November 2017
Accepts healthy volunteers No
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria:

- Able and willing to participate in this study

- Availability of signed informed consent

- Healthy, not on any medication

- Able to provide a breath sample

- Having a condition (eg. suspected strep throat, MRSA, C difficile) which would require a swab/sample for culture

Exclusion Criteria:

- Under the age of 6years

- Eating food or drink (excluding water) within 2 hours of breath test time

- Pregnant or Breastfeeding

- Chronic Obstructive Pulmonary Disease (COPD)

- Inability to comply with study procedure/unable to follow directions

- Currently taking antibiotics or other medication (excluding analgesics)

Study Design


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
BreathTec Biomedical Inc.

References & Publications (3)

Bos LD, Sterk PJ, Schultz MJ. Volatile metabolites of pathogens: a systematic review. PLoS Pathog. 2013 May;9(5):e1003311. doi: 10.1371/journal.ppat.1003311. Epub 2013 May 9. Review. — View Citation

Jünger M, Vautz W, Kuhns M, Hofmann L, Ulbricht S, Baumbach JI, Quintel M, Perl T. Ion mobility spectrometry for microbial volatile organic compounds: a new identification tool for human pathogenic bacteria. Appl Microbiol Biotechnol. 2012 Mar;93(6):2603-14. doi: 10.1007/s00253-012-3924-4. Epub 2012 Feb 12. — View Citation

Thorn RM, Greenman J. Microbial volatile compounds in health and disease conditions. J Breath Res. 2012 Jun;6(2):024001. doi: 10.1088/1752-7155/6/2/024001. Epub 2012 May 4. Review. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Evidence of Infection detected by exhaled breath analysis confirmed by laboratory culture Within 3 to 7 days of obtaining culture and exhaled breath sample
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