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Clinical Trials/CTRI/2024/02/062929
CTRI/2024/02/062929
Completed
Phase 4

A post market clinical follow up prospective study to evaluate safety and performance of Sodium Hyaluronate 0.2% Eye Drops - NI

Amanta Healthcare Limited0 sites54 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Health Condition 1: H579- Unspecified disorder of eye and adnexa
Sponsor
Amanta Healthcare Limited
Enrollment
54
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 4, 2024
Last Updated
last year
Study Type
Pms

Investigators

Eligibility Criteria

Inclusion Criteria

  • Subjects who are able to give voluntary, written informed consent to participate in this study.
  • Subjects who experience eye dryness, Eye Soreness/ burning, Irritative Sensation, Eye fatigue, contact lens caused dryness, discomfort of eyes due to the continuous use of computer/ TV/
  • exposed pollution/ dry environment

Exclusion Criteria

  • Anyone with known allergic reaction to Sodium Hyaluronate 0\.2% Eye Drops.
  • Subjects with existing eye infection
  • History of ocular surgery. History or active signs of severe or serious ocular conditions such as inflammatory corneal ulcers, recurrent erosions, and uveitis at any time
  • Patients participating in any another clinical trial during study
  • Pregnant/lactating women during study period.

Outcomes

Primary Outcomes

Not specified

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