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

NCT02956330 · ClinicalTrials.gov registry record

Retrospective Study of the Safety and Efficacy of Patients With RVO in Subjects Who Completed Parent Study CLS1003-201

A clinical trial, sponsored by Clearside Biomedical.

Completed
Registry status
20
Enrollment target

NCT02956330: Completed study, sponsored by Clearside Biomedical.

NCT02956330 is a clinical trial that has completed, run by Clearside Biomedical. The registered enrollment target is 20 participants. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02956330 has completed, sponsored by Clearside Biomedical.

COMPLETED
Registry status
20 participants
Enrollment target

Study Summary

The purpose of this non interventional retrospective study is to continue to collect data from patients following their completion of Protocol CLS 1003-201: "Safety and Efficacy of Suprachoroidal CLS-TA with Intravitreal Aflibercept in Subjects with Macular Edema Following Retinal Vein Occlusion" (ie, the parent study).

Trial Details

FieldValue
Enrollment Target 20 participants
Start Date 2016-11
Est. Completion 2017-04-12
Clearside Biomedical

14 total trials

What the finished NCT02956330 record still lists

NCT02956330 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 20 participants, a relatively small participant target.

The record links to 0 conditions, and to 0 interventions.

NCT02956330 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02956330 about?

NCT02956330 is a clinical study titled "Retrospective Study of the Safety and Efficacy of Patients With RVO in Subjects Who Completed Parent Study CLS1003-201". The purpose of this non interventional retrospective study is to continue to collect data from patients following their completion of Protocol CLS 1003-201: "Safety and Efficacy of Suprachoroidal CLS-TA with Intravitreal Aflibercept in Subjects with Macular Edema Following Retinal Vein Occlusion" (i...

What is the current status of trial NCT02956330?

This trial is currently completed. The enrollment target is 20 participants. The study started on 2016-11. Estimated completion is 2017-04-12.

Who is sponsoring clinical trial NCT02956330?

This trial is sponsored by Clearside Biomedical, which has 14 total clinical trials registered on ClinicalTrials.gov.

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

  • NCT00573339 · 20 participants

    Cardiac Magnetic Resonance Imaging (MRI) Normal Reference Control Group Testing

  • NCT00692939 · 20 participants · Phase 1

    Autologous Stem Cell Transplantation for Crohn's Disease

  • NCT00967785 · 20 participants · Phase 1

    A Phase I Study of Mozobil in the Treatment of Patients With WHIMS

  • NCT01406691 · 20 participants · Phase 4

    Light Flashes to Treat Delayed Sleep Phase Disorder (DSPD)

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02956330, the US trial registry maintained by the National Library of Medicine. NCT02956330 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.