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NCT00699803 Clinical Trial

Study of T-PRED(TM) Compared to Pred Forte(R)

Cataract Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00699803
Other study ID # CL-PKT-0312081-P
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date May 2008
Est. completion date August 2008

Study information
Verified date September 2020
Source Bausch & Lomb Incorporated
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Study of T-PRED(TM) compared to Pred Forte(R)

Recruitment information / eligibility
Status Completed
Enrollment 64
Est. completion date August 2008
Est. primary completion date August 2008
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- 18 years of age

Exclusion Criteria:

- No active or adverse disease

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• T-PRED
T-PRED sterile ophthalmic solution
• Pred Forte
Pred Forte sterile ophthalmic solution

Locations
Country Name City State
United States ISTA Pharmaceuticals, Inc. Irvine California

Sponsors (1)
Lead Sponsor Collaborator
Bausch & Lomb Incorporated

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Mean Aqueous Humor Prednisolone Acetate Concentration 4 hours
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