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NCT04542616 · ClinicalTrials.gov registry record · NA

Baerveldt 350 vs Ahmed ClearPath 250 for the Treatment of Glaucoma

A NA study of Glaucoma, sponsored by State University of New York at Buffalo.

Completed
Registry status
NA
Development phase
80
Enrollment target
1
Study location

NCT04542616: Completed NA study of Glaucoma, sponsored by State University of New York at Buffalo.

NCT04542616 is a NA study of Glaucoma that has completed, run by State University of New York at Buffalo. The registered enrollment target is 80 participants, below the 910-participant average among 92 other Glaucoma trials with a reported enrollment target (91% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04542616, a NA study of Glaucoma, has completed, sponsored by State University of New York at Buffalo.

COMPLETED
Registry status
NA
Development phase
80 participants
Enrollment target
1
Study location

Study Summary

To compare the safety and efficacy of Baerveldt 350 and Ahmed ClearPath 250 tube shunts in lowering IOP in glaucoma patients.

Primary Outcome

Mean IOP in each treatment group at the above time points

Conditions Studied

Interventions

  • DEVICE Baerveldt 350 vs. Ahmed ClearPath 250 tube shunt implantation

Study Locations (1)

New York

  • The Ira G. Ross Eye Institute - Buffalo

Trial Details

FieldValue
Enrollment Target 80 participants
Start Date 2020-08-13
Est. Completion 2024-07-31
Phase NA

What the finished NCT04542616 record still lists

NCT04542616 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 80 participants, a relatively small participant target, below the 910-participant average among 92 other Glaucoma trials with a reported enrollment target (91% lower).

The record links to 1 condition, with Glaucoma appearing as the primary indexed condition, and to 1 intervention - of which Baerveldt 350 vs. Ahmed ClearPath 250 tube shunt implantation is the first listed.

NCT04542616 reports a single indexed study location in New York.

Frequently Asked Questions

What is clinical trial NCT04542616 about?

NCT04542616 is a clinical study titled "Baerveldt 350 vs Ahmed ClearPath 250 for the Treatment of Glaucoma". To compare the safety and efficacy of Baerveldt 350 and Ahmed ClearPath 250 tube shunts in lowering IOP in glaucoma patients.

What is the current status of trial NCT04542616?

This trial is currently completed. It is a NA study. The enrollment target is 80 participants. The study started on 2020-08-13. Estimated completion is 2024-07-31.

What conditions does trial NCT04542616 study?

This clinical trial studies the following conditions: Glaucoma.

What interventions are being tested in trial NCT04542616?

The interventions under investigation include: Baerveldt 350 vs. Ahmed ClearPath 250 tube shunt implantation (DEVICE).

Who is sponsoring clinical trial NCT04542616?

This trial is sponsored by State University of New York at Buffalo, which has 243 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04542616 being conducted?

This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Glaucoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT04542616's enrollment target sits among peer trials

80 50th of 92 higher than 43 of 92 other Glaucoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Glaucoma 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 NCT04542616, the US trial registry maintained by the National Library of Medicine. NCT04542616 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.