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NCT07113210 · ClinicalTrials.gov registry record · Phase 4

Quality of Life in Presbyopic Patients Who Are Treated With Qlosi

A Phase 4 study of Dry Eye and Presbyopia, sponsored by Southern College of Optometry.

Recruiting
Registry status
Phase 4
Development phase
36
Enrollment target
2
Study locations

NCT07113210: Recruiting Phase 4 study of Dry Eye and Presbyopia, sponsored by Southern College of Optometry.

NCT07113210 is a Phase 4 study of Dry Eye and Presbyopia that is actively recruiting participants, run by Southern College of Optometry. The registered enrollment target is 36 participants, below the 95-participant average among 41 other Dry Eye trials with a reported enrollment target (62% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07113210, a Phase 4 study of Dry Eye and Presbyopia, is actively recruiting participants, sponsored by Southern College of Optometry.

RECRUITING
Registry status
Phase 4
Development phase
36 participants
Enrollment target
2
Study locations

Study Summary

The goal of this clinical trial is to determine how Qlosi™ (pilocarpine HCL ophthalmic solution) 0.4%impacts the quality of life of participants with presbyopia by using a battery of validated and investigator-developed instruments * Improvement in presbyopic symptoms as measured with the Near Activity Visual Questionnaire-Presbyopia (NAVQ-P) when using Qlosi™ at week 4 compared to baseline (continuous variable). * Improvement in presbyopic symptoms as measured with the Visual Quality of Life with Time Survey (VisQualT) questionnaire when using Qlosi™ at week 4 compared to baseline.

Primary Outcome

• Improvement in presbyopic symptoms as measured with the Near Activity Visual Questionnaire-Presbyopia (NAVQ-P) when using Qlosi at week 4 compared to baseline (continuous variable). In which higher scores are better.

Interventions

  • DRUG pilocarpine HCL ophthalmic solution

Study Locations (2)

Minnesota

  • Complete Eye Care of Medina - Medina

Tennessee

  • The Southern College of Optometry - Memphis

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2025-07-18
Est. Completion 2025-11-15
Phase Phase 4
Southern College of Optometry

11 total trials

What NCT07113210 shows while recruiting

NCT07113210 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 95-participant average among 41 other Dry Eye trials with a reported enrollment target (62% lower).

The record links to 3 conditions, with Dry Eye appearing as the primary indexed condition, and to 1 intervention - of which pilocarpine HCL ophthalmic solution is the first listed.

NCT07113210 reports a single indexed study location in Minnesota, Tennessee.

Frequently Asked Questions

What is clinical trial NCT07113210 about?

NCT07113210 is a clinical study titled "Quality of Life in Presbyopic Patients Who Are Treated With Qlosi". The goal of this clinical trial is to determine how Qlosi™ (pilocarpine HCL ophthalmic solution) 0.4%impacts the quality of life of participants with presbyopia by using a battery of validated and investigator-developed instruments * Improvement in presbyopic symptoms as measured with the Near Acti...

What is the current status of trial NCT07113210?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 36 participants. The study started on 2025-07-18. Estimated completion is 2025-11-15.

What conditions does trial NCT07113210 study?

This clinical trial studies the following conditions: Dry Eye, Presbyopia, Glasses.

What interventions are being tested in trial NCT07113210?

The interventions under investigation include: pilocarpine HCL ophthalmic solution (DRUG).

Who is sponsoring clinical trial NCT07113210?

This trial is sponsored by Southern College of Optometry, which has 11 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07113210 being conducted?

This trial has 2 study locations across Minnesota, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Dry Eye

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 NCT07113210's enrollment target sits among peer trials

36 27th of 41 higher than 14 of 41 other Dry Eye trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Dry Eye 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 NCT07113210, the US trial registry maintained by the National Library of Medicine. NCT07113210 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.