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NCT07155057 · ClinicalTrials.gov registry record · NA

Evaluating Crosslinked Hyaluronate Canalicular Gel for the Treatment of DED in Patients Undergoing Cataract Surgery

A NA study of Dry Eye Disease (DED), sponsored by Vance Thompson Vision.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT07155057 is a NA study of Dry Eye Disease (DED) that is actively recruiting participants, run by Vance Thompson Vision. The registered enrollment target is 60 participants, below the 471-participant average among 3 other Dry Eye Disease (DED) trials with a reported enrollment target (87% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT07155057, a NA study of Dry Eye Disease (DED), is actively recruiting participants, sponsored by Vance Thompson Vision.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

To review how patients report using a hyaluronate crosslinked canalicular gel placed before cataract surgery

Conditions Studied

Interventions

  • DEVICE Cross-Linked Hyaluronate Gel Prefilled Syringe 30 MG/3ML

Study Locations (1)

South Dakota

  • Vance Thompson Vision Clinic, Prof. LLC - Sioux Falls

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2025-09-03
Est. Completion 2026-12
Phase NA

Sponsor

Vance Thompson Vision

14 total trials

What the Registry Record Tells You About NCT07155057

The ClinicalTrials.gov registry entry for NCT07155057 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 471-participant average among 3 other Dry Eye Disease (DED) trials with a reported enrollment target (87% lower). The listed sponsor is Vance Thompson Vision, which has 14 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Dry Eye Disease (DED) appearing as the primary indexed condition, and to 1 intervention - of which Cross-Linked Hyaluronate Gel Prefilled Syringe 30 MG/3ML is the first listed.

NCT07155057 reports 1 study location spanning 1 distinct geographic area - top geographies include South Dakota.

Frequently Asked Questions

What is clinical trial NCT07155057 about?

NCT07155057 is a clinical study titled "Evaluating Crosslinked Hyaluronate Canalicular Gel for the Treatment of DED in Patients Undergoing Cataract Surgery". To review how patients report using a hyaluronate crosslinked canalicular gel placed before cataract surgery

What is the current status of trial NCT07155057?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2025-09-03. Estimated completion is 2026-12.

What conditions does trial NCT07155057 study?

This clinical trial studies the following conditions: Dry Eye Disease (DED).

What interventions are being tested in trial NCT07155057?

The interventions under investigation include: Cross-Linked Hyaluronate Gel Prefilled Syringe 30 MG/3ML (DEVICE).

Who is sponsoring clinical trial NCT07155057?

This trial is sponsored by Vance Thompson Vision, which has 14 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07155057 being conducted?

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

Similar trials for Dry Eye Disease (DED)

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

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