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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01817478
Other study ID # 0093-12-ZIV
Secondary ID
Status Recruiting
Phase N/A
First received March 18, 2013
Last updated March 22, 2013
Start date January 2013
Est. completion date December 2013

Study information

Verified date March 2013
Source Ziv Hospital
Contact Joseph Pikkel, M.D
Email pikel.y@ziv.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

The investigators want to find out if there is any difference between the microbiotic flora lining the conjunctiva of medical staff that work in the hospital and others who do not work in the hospital.


Recruitment information / eligibility

Status Recruiting
Enrollment 90
Est. completion date December 2013
Est. primary completion date June 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- healthy medical workers.

Exclusion Criteria:

- any ocular disease.

- previous ocular surgery.

Study Design

Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
microbiologic sample


Locations

Country Name City State
Israel Ziv Medical Center Safed

Sponsors (1)

Lead Sponsor Collaborator
Ziv Hospital

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary significant difference in the bacterial flora of conjunctiva 12 months No
See also
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Completed NCT00575380 - Study of AzaSite Versus Vigamox Concentrations in the Conjunctiva and Aqueous Humor in Subjects Undergoing Routine Cataract Surgery Phase 4
Completed NCT00564447 - Study of AzaSite (Azithromycin) Versus Vigamox in the Conjunctiva of Healthy Volunteers Phase 4
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