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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02912520
Other study ID # ORV001
Secondary ID
Status Completed
Phase N/A
First received September 13, 2016
Last updated April 23, 2017
Start date June 2016
Est. completion date April 23, 2017

Study information

Verified date April 2017
Source Medical University of Vienna
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Investigators hypothesize that Immunoglobine (Ig) production is influenced by the microbiota of the gut. Investigators will compare microbiota-dependent Ig production in the bronchoalveolar lavage fluid of patients with and without antibiotic therapy in order to detect significant differences.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date April 23, 2017
Est. primary completion date April 23, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- endotracheal intubation

- antibiotic therapy for 2 weeks OR no antibiotic therapy for at least 3 months

Exclusion Criteria:

- active infection

- pregnancy

- immunodeficiency

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Anti-Bacterial Agents
administration of any antibiotic substance(s) over the course of 2 weeks

Locations

Country Name City State
Austria Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

References & Publications (1)

Hoogkamp-Korstanje JA, de Koning J, Heesemann J, Festen JJ, Houtman PM, van Oyen PL. Influence of antibiotics on IgA and IgG response and persistence of Yersinia enterocolitica in patients with Yersinia-associated spondylarthropathy. Infection. 1992 Mar-Apr;20(2):53-7. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary IgA levels in the bronchoalveolar lavage fluid 2 weeks of ICU stay
Secondary number of detected bacterial, viral, and fungal infections per patient through study completion, an average of 2 months
See also
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