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NCT00798317 · ClinicalTrials.gov registry record · Phase 3

Trial of Microplasmin Intravitreal Injection for Non-Surgical Treatment of Focal Vitreomacular Adhesion. The MIVI-TRUST (TG-MV-007) Trial.

A Phase 3 study, sponsored by ThromboGenics.

Completed
Registry status
Phase 3
Development phase
326
Enrollment target

NCT00798317: Completed Phase 3 study, sponsored by ThromboGenics.

NCT00798317 is a Phase 3 study that has completed, run by ThromboGenics. The registered enrollment target is 326 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (58% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00798317, a Phase 3 study, has completed, sponsored by ThromboGenics.

COMPLETED
Registry status
Phase 3
Development phase
326 participants
Enrollment target

Study Summary

This trial will evaluate the safety and efficacy of microplasmin, administered as an intravitreal injection, in subjects with focal vitreomacular adhesion. In previously performed clinical trials, some patients treated with intravitreal microplasmin have had resolution of their underlying condition, including macular hole closure, without need for vitrectomy. This clinical trial is justified because the sponsor believes the potential benefits outweigh the potential risks.

Primary Outcome

Proportion of subjects with nonsurgical resolution of focal vitreomacular adhesion at Day 28, as determined by masked Central Reading Centre (CRC) Optical Coherence Tomography(OCT)evaluation.

Interventions

  • DRUG Placebo
  • DRUG Ocriplasmin 125µg

Trial Details

FieldValue
Enrollment Target 326 participants
Start Date 2008-12
Est. Completion 2010-07
Phase Phase 3
ThromboGenics

12 total trials

What the finished NCT00798317 record still lists

NCT00798317 is an interventional study that assigns participants to a tested intervention. The registered 326 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (58% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00798317 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00798317 about?

NCT00798317 is a clinical study titled "Trial of Microplasmin Intravitreal Injection for Non-Surgical Treatment of Focal Vitreomacular Adhesion. The MIVI-TRUST (TG-MV-007) Trial.". This trial will evaluate the safety and efficacy of microplasmin, administered as an intravitreal injection, in subjects with focal vitreomacular adhesion. In previously performed clinical trials, some patients treated with intravitreal microplasmin have had resolution of their underlying condition,...

What is the current status of trial NCT00798317?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 326 participants. The study started on 2008-12. Estimated completion is 2010-07.

What interventions are being tested in trial NCT00798317?

The interventions under investigation include: Placebo (DRUG), Ocriplasmin 125µg (DRUG).

Who is sponsoring clinical trial NCT00798317?

This trial is sponsored by ThromboGenics, which has 12 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00798317's enrollment target sits among peer trials

326 1075th of 2000 higher than 925 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00798317, the US trial registry maintained by the National Library of Medicine. NCT00798317 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.