Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02700984 · ClinicalTrials.gov registry record · NA

A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS Trial

A NA study, sponsored by Alcon Research.

Completed
Registry status
NA
Development phase
282
Enrollment target

NCT02700984: Completed NA study, sponsored by Alcon Research.

NCT02700984 is a NA study that has completed, run by Alcon Research. The registered enrollment target is 282 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02700984, a NA study, has completed, sponsored by Alcon Research.

COMPLETED
Registry status
NA
Development phase
282 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the long-term safety of the CyPass Micro-Stent in subjects who completed Study Protocol TMI-09-01, COMPASS Trial.

Primary Outcome

Sight-threatening adverse events occurring in the study eye included, but were not limited to: BCVA loss of ≥ 3 lines, endophthalmitis, corneal decompensation, severe retinal detachment, severe choroidal hemorrhage, severe choroidal detachment and aqueous misdirection. The number of events at the end of Year 5 was divided by the number of eyes at risk at the beginning of Year 1 for a 5-year annualized rate. The 5-year annualized rate is reported as a percentage, with the last annual non-censored

Interventions

  • PROCEDURE Cataract Surgery
  • DEVICE CyPass Micro-Stent

Trial Details

FieldValue
Enrollment Target 282 participants
Start Date 2016-03-30
Est. Completion 2018-04-18
Phase NA
Alcon Research

275 total trials

What the finished NCT02700984 record still lists

NCT02700984 is an interventional study that assigns participants to a tested intervention. The registered 282 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (80% lower).

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

NCT02700984 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02700984 about?

NCT02700984 is a clinical study titled "A Study to Assess Long-Term Safety of the CyPass Micro-Stent in Patients Completing the COMPASS Trial". The purpose of this study is to evaluate the long-term safety of the CyPass Micro-Stent in subjects who completed Study Protocol TMI-09-01, COMPASS Trial.

What is the current status of trial NCT02700984?

This trial is currently completed. It is a NA study. The enrollment target is 282 participants. The study started on 2016-03-30. Estimated completion is 2018-04-18.

What interventions are being tested in trial NCT02700984?

The interventions under investigation include: Cataract Surgery (PROCEDURE), CyPass Micro-Stent (DEVICE).

Who is sponsoring clinical trial NCT02700984?

This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02700984's enrollment target sits among peer trials

282 379th of 2000 higher than 1,621 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT02860364 · 282 participants · NA

    Comparing Hypothermic Temperatures During Hemiarch Surgery

  • NCT04867395 · 282 participants · NA

    A Multi-Phase Study Examining Hospital to Home Transitions for Children With Medical Complexity

  • NCT05101070 · 282 participants · Phase 1

    S-531011 as Monotherapy and in Combination With an Immune Checkpoint Inhibitor in Advanced or Metastatic Solid Tumors

  • NCT06276491 · 282 participants · Phase 1

    Phase 1, Safety and Tolerability Study of XmAb541 in Advanced Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02700984, the US trial registry maintained by the National Library of Medicine. NCT02700984 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.