ClinicalTrials.gov record
Completed Phase 2 Interventional Results available

A Study of the Safety and Efficacy of Microplasmin to Induce a Posterior Vitreous Detachment (MIVI III)

ClinicalTrials.gov ID: NCT00412958

Public ClinicalTrials.gov record NCT00412958. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 12, 2026, 10:08 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Placebo-Controlled, Double-Masked, Parallel Group, Dose-Ranging Clinical Trial of Intravitreal Microplasmin in Patients Undergoing Surgical Vitrectomy: The MIVI III (Microplasmin For Vitreous Injection III) Trial

Study identification

NCT ID
NCT00412958
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
ThromboGenics
Industry
Enrollment
125 participants

Conditions and interventions

Conditions

Interventions

  • Ocriplasmin 125µg Drug
  • Ocriplasmin 25µg Drug
  • Ocriplasmin 75µg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2006
Primary completion
Sep 30, 2008
Completion
Sep 30, 2008
Last update posted
Dec 16, 2014

2006 – 2008

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
19
Facility City State ZIP Site status
Retina Centers, P.C. Tucson Arizona 85704
VMR Institute Huntington Beach California 92647
Jules Stein Eye Institute/UCLA Los Angeles California 90095
Retinal Consultants of San Diego Poway California 92064
Retinal Consultants Medical Group Sacramento California 95819
National Ophtlamic Research Institute Fort Meyers Florida 33912
Center for Retina and Macular Disease Winter Haven Florida 33880
Rush University Med. Ctr Chicago Illinois 60612
Mailing add: New England Eye Center - Tufts Boston Massachusetts 02111
Associated Retinal Consultants, P.C. Royal Oak Michigan 48073
Vitroretinal Surgery, PA Minneapolis Minnesota 55435
Retina Vitreous Centre, PA New Brunswick New Jersey 08901
Columbia University - Harkness Eye Institute New York New York 10032
Retina Vitreous Surgeons of Central NY New York New York 13224
Duke Eye Center Durham North Carolina 27710
Retina Association of Cleveland Lakewood Ohio 44107
Allegheny Ophthalmic & Orbital Associates, P.C. Pittsburgh Pennsylvania 15212
Vanderbilt Eye Institute Nashville Tennessee 37232-8808
Vitreoretinal Consultants Houston Texas 77030
Valley Retina Institute, P.A. McAllen Texas 78503

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00412958, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 16, 2014 · Synced May 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00412958 live on ClinicalTrials.gov.

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