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Dietary Supplement

Nutritears® for Dry Eye Syndrome

N/A
Waitlist Available
Research Sponsored by Applied Science & Performance Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, day 14, day 28, day 56
Awards & highlights

Study Summary

This trial will test whether a dietary supplement called Nutritears is effective and safe for people with dry eye syndrome. People in the trial will take the supplement every morning for 8 weeks.

Eligible Conditions
  • Dry Eye Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, day 14, day 28, day 56
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline, day 14, day 28, day 56 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Ocular Surface Disease Index (OSDI) score
Schirmer's Test (without anesthesia)
Secondary outcome measures
Corneal and Conjunctival Staining
MMP-9
Rescue Medication Use
+3 more
Other outcome measures
Changes in Alanine Transaminase levels
Changes in Albumin levels
Changes in Albumin to Globulin ratio
+35 more

Trial Design

2Treatment groups
Experimental Treatment
Placebo Group
Group I: Dietary supplementExperimental Treatment1 Intervention
Consume one capsule every morning after the breakfast at the same time every day for 56 days
Group II: PlaceboPlacebo Group1 Intervention
Consume one capsule every morning after the breakfast at the same time every day for 56 days
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Nutritears®
2022
N/A
~140

Find a Location

Who is running the clinical trial?

True Eye Experts - LutzUNKNOWN
True Eye Experts - New TampaUNKNOWN
1 Previous Clinical Trials
15 Total Patients Enrolled
True Eye Experts - South TampaUNKNOWN

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What is the maximum capacity of participants allowed in this research endeavor?

"Indeed, there is evidence hosted on clinicaltrials.gov that confirms the active recruitment of participants for this medical study which was initially shared on August 15th 2022. Currently 124 volunteers are being sought from 3 separate sites with it's latest update occurring September 8th 2022."

Answered by AI

What is the primary focus of this research endeavor?

"The primary monitored outcome in this study is the Ocular Surface Disease Index (OSDI). Secondary objectives analysed include corneal and conjunctival staining, MMP-9 levels, and tear osmolarity. Corneal and conjunctival staining will be measured using a modified Oxford score from 0 to 5; InflammaDry MMP-9 kits are used for qualitative determination of MMP-9 presence; Tear osmolarity refers to measurements of osmotically active particles which should not exceed 300 milliosmole/L. Measurements will occur at Baseline, Day 14,"

Answered by AI

Does this research team accept geriatric participants?

"According to the inclusion parameters spelled out in this clinical trial, potential participants must fall between 18 and 65 years of age."

Answered by AI

Are there still vacancies for participants in this research project?

"Correct. The details on clinicaltrials.gov suggest that this trial is still recruiting participants, with the initial posting dated August 15th 2022 and a recent update to the information occurring on September 8th 2022."

Answered by AI

Are there any requirements to participate in this medical experiment?

"To join this medical trial, patients must have a diagnosis of dry eye and be aged between 18-65. In total, the research team is looking for 124 participants."

Answered by AI
~49 spots leftby Apr 2025