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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00569881
Other study ID # Donnenfeld2
Secondary ID
Status Completed
Phase N/A
First received December 6, 2007
Last updated December 7, 2007
Start date January 2007
Est. completion date March 2007

Study information

Verified date December 2007
Source Donnenfeld, Eric, M.D.
Contact n/a
Is FDA regulated No
Health authority United States: None Needed
Study type Observational

Clinical Trial Summary

The prescribed antibiotic for prophylaxis of infection following PRK should be effective at eradicating a potential infection. In addition, the antibiotic should have a rapid onset of action, effectively penetrate the target tissue, and be safe and not toxic to any layer of the healing cornea, especially the epithelium. Several studies have investigated the toxicity of the fourth generation fluoroquinolones on the corneal epithelium and studies have demonstrated that gatifloxacin is less deleterious to the healing cornea than moxifloxacin. Most of these studies, however, have been conducted in animals. This was a retrospective chart review.


Description:

Prior generation fluoroquinolones predominantly either inhibit topoisomerase II (DNA Gyrase) or topoisomerase IV and therefore only require one genetic mutation for bacteria to develop resistance. Fourth-generation fluoroquinolones are equally effective against topoisomerase II and IV, which significantly expands their spectrum of action against gram-positive agents and atypical mycobacteria and Nocardia . This duality of action of the fourth generation fluoroquinolones requires that for bacteria to become resistant to these agents, the bacteria must undergo two genetic mutations resulting in a significantly decreased chance of an organism developing resistance.Minimum inhibitory concentrations determined in vitro suggest that fourth-generation fluoroquinolones are more effective than second- and third-generation fluoroquinolones against gram-positive bacteria including Staphylococcal species found in endophthalmitis and bacterial keratitis cultures. The increased efficacy of fourth-generation fluoroquinolones make these antibiotics important agents to evaluate for prophylaxis against post-PRK infections. This was a retrospective chart review.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date March 2007
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients were eligible for inclusion if they were a healthy male or female 18 years of age or older and were candidates for bilateral PRK.

- Eligible patients had a best-corrected Early Treatment of Diabetic Retinopathy Study (ETDRS) visual acuity score equivalent to a Snellen score of 20/30 or better in each eye, had a stable prescription for 1 year, were willing to participate in the study, and were able to comprehend and sign the informed consent form.

- All subjects were instructed that if they decide not to participate they could withdraw from the study at any time.

Exclusion Criteria:

- Patients were excluded from the study if they had a history of refractive or other ocular surgery in either eye.

- Patients with any condition which could delay wound healing were not eligible to participate.

- They were excluded if they had poor tolerance to any component of the masked study fluoroquinolones, AcularĀ® LS (Allergan) or Pred ForteĀ® (Allergan).

- Patients were also excluded if they required the use of a systemic antibiotic during the study period, were involved in another investigational study or had participated in a study within 30 days prior to the start of this study.

Study Design

Observational Model: Case Control, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Drug:
gatifloxacin and moxifloxacin
Comparison of wound healing between drugs

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Donnenfeld, Eric, M.D.

Outcome

Type Measure Description Time frame Safety issue
Primary Wound Healing Days after PRK No
See also
  Status Clinical Trial Phase
Completed NCT00681642 - Corneal Epithelial Wound Healing Difference Between Human Autoserum and Cord Blood Serum N/A