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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00410891
Other study ID # 96803 (eProtocol 4384)
Secondary ID
Status Completed
Phase Phase 4
First received October 2, 2006
Last updated October 4, 2017
Start date July 2008
Est. completion date December 2009

Study information

Verified date October 2017
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluation of efficacy of topical preoperative antibiotics in patients undergoing intravitreous injections.


Recruitment information / eligibility

Status Completed
Enrollment 129
Est. completion date December 2009
Est. primary completion date December 2009
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- intravitreous injection

Exclusion Criteria:

- antibiotic use

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
gatifloxacin


Locations

Country Name City State
United States Stanford Stanford California

Sponsors (1)

Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Positive Culture The percentage of patients with a positive bacterial culture following administration of study treatment is presented. Study day 1, assessed following administration of study treatment
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