# Randomized Single Center Study to Evaluate Tolerability, Symptoms, and Visual Functional Outcomes With the Use of OTC Lubricating Eye Drops in Subjects With Dry Eye Disease

> **NCT07676084** · PHASE4 · RECRUITING · sponsor: **Andover Research Eye Institute** · enrollment: 60 (estimated)

## Conditions studied

- Dry Eye Disease (DED)

## Interventions

- **DRUG:** Preservative Free Polyethylene glycol 400 0.25%
- **DRUG:** Propylene Glycol (0.6%)
- **DRUG:** Carboxymethylcellulose sodium 0.5%, Glycerin 1.0%, Polysorbate 80 0.5%

## Key facts

- **NCT ID:** NCT07676084
- **Lead sponsor:** Andover Research Eye Institute
- **Sponsor class:** INDUSTRY
- **Phase:** PHASE4
- **Study type:** INTERVENTIONAL
- **Status:** RECRUITING
- **Start date:** 2026-06-03
- **Primary completion:** 2026-10
- **Final completion:** 2026-12
- **Target enrollment:** 60 (ESTIMATED)
- **Last updated:** 2026-06-30


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT07676084

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT07676084, "Randomized Single Center Study to Evaluate Tolerability, Symptoms, and Visual Functional Outcomes With the Use of OTC Lubricating Eye Drops in Subjects With Dry Eye Disease". Retrieved via MORVS 2026-10-20 from https://api.morvs.ai/clinical/NCT07676084. Licensed CC0.

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*[Clinical trials dataset](/datasets/clinical-trials) · CC0 1.0*