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Sponsored by: |
Bausch & Lomb, Inc. |
Information provided by: | Bausch & Lomb, Inc. |
ClinicalTrials.gov Identifier: | NCT00348439 |
Plasmin is expected to create a posterior vitreous detachment. The pharmacological creation of a posterior vitreous detachment may be beneficial in a variety of conditions.
Condition | Intervention | Phase |
Disorders Caused by Vitreo-Retinal Traction. |
Drug: Plasmin |
Phase II |
ChemIDplus related topics: | Fibrinolysin, human |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Bausch & Lomb, Inc. ( Marcia de Souza Lima ) |
Study ID Numbers: | 437 |
First Received: | June 30, 2006 |
Last Updated: | May 12, 2008 |
ClinicalTrials.gov Identifier: | NCT00348439 |
Health Authority: | United States: Food and Drug Administration |
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