Autopsy report · NCT00804726

Evaluation of the Safety and Effectiveness of the Akreos MI Five-0 Intraocular Lens.

Cause of deathFutility Automatic label, confidence 0.5, unverified. How labels are made.

“Test lens did not meet near visual efficacy endpoints”

The sponsor’s own words in the registry.

Life of this trial

Ran for about 1 year 8 months before it stopped.
10 participants enrolled.
No results are posted on the registry.

Vital statistics

Status: Terminated
Phase: Na
Sponsor: Bausch & Lomb Incorporated
Sponsor type: Industry
Conditions: Cataract
Interventions: Akreos MI Five-O
Participants: 10
Sites: 1
Countries: Germany

Look deeper

The official registry record (the source of truth)
Record history: every change the sponsor made
Open it in the database

Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.