# A Study to Evaluate the Safety and Effectiveness Assessments of Restylane-Defyne for Punctual Occlusion

> **NCT04022382** · NA · COMPLETED · sponsor: **John C Meyer, MD** · enrollment: 17 (actual)

## Conditions studied

- Dry Eye

## Interventions

- **DEVICE:** Restylane Defyne

## Key facts

- **NCT ID:** NCT04022382
- **Lead sponsor:** John C Meyer, MD
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2019-07-18
- **Primary completion:** 2019-08-26
- **Final completion:** 2019-08-26
- **Target enrollment:** 17 (ACTUAL)
- **Last updated:** 2019-09-06


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT04022382

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT04022382, "A Study to Evaluate the Safety and Effectiveness Assessments of Restylane-Defyne for Punctual Occlusion". Retrieved via AI Analytics 2026-05-27 from https://api.ai-analytics.org/clinical/NCT04022382. Licensed CC0.

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