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NCT04527887 · ClinicalTrials.gov registry record · Phase 4

Intracanalicular Dexamethasone Insert for the Treatment of Inflammation and Discomfort in Dry Eye Disease (DEcIDED)

A Phase 4 study, sponsored by Tufts Medical Center.

Terminated
Registry status
Phase 4
Development phase
54
Enrollment target

NCT04527887 is a Phase 4 study that was terminated before completion, run by Tufts Medical Center. The registered enrollment target is 54 participants.

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The verdict

NCT04527887, a Phase 4 study, was terminated before completion, sponsored by Tufts Medical Center.

TERMINATED
Registry status
Phase 4
Development phase
54 participants
Enrollment target

Study Summary

This prospective, single-center, randomized, double-masked, parallel comparison, sponsored study seeks to investigate the efficacy of Intracanalicular dexamethasone Insert (IDI) on ameliorating the signs and symptoms of dry eye disease.

Interventions

  • DRUG Dextenza (IDI) (Sustained Release Dexamethasone), (0.4 mg)
  • OTHER ProLong™ collagen plugs

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2020-09-04
Est. Completion 2024-12-31
Phase Phase 4

Sponsor

Tufts Medical Center

169 total trials

What the Registry Record Tells You About NCT04527887

The ClinicalTrials.gov registry entry for NCT04527887 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Tufts Medical Center, which has 169 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Dextenza (IDI) (Sustained Release Dexamethasone), (0.4 mg) is the first listed.

NCT04527887 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT04527887 about?

NCT04527887 is a clinical study titled "Intracanalicular Dexamethasone Insert for the Treatment of Inflammation and Discomfort in Dry Eye Disease (DEcIDED)". This prospective, single-center, randomized, double-masked, parallel comparison, sponsored study seeks to investigate the efficacy of Intracanalicular dexamethasone Insert (IDI) on ameliorating the signs and symptoms of dry eye disease.

What is the current status of trial NCT04527887?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 54 participants. The study started on 2020-09-04. Estimated completion is 2024-12-31.

What interventions are being tested in trial NCT04527887?

The interventions under investigation include: Dextenza (IDI) (Sustained Release Dexamethasone), (0.4 mg) (DRUG), ProLong™ collagen plugs (OTHER).

Who is sponsoring clinical trial NCT04527887?

This trial is sponsored by Tufts Medical Center, which has 169 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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