Last reviewed · How we verify
NCT05481450
Efficacy and Safety Safety of Nutritears® in Adults With Dry Eye Syndrome
NA trial testing Nutritears® in Dry Eye in 131 participants. Completed in 22 May 2023.
15 May 2023
Quick facts
| Lead sponsor | Applied Science & Performance Institute |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | quadruple |
| Primary purpose | treatment |
| Enrollment | 131 |
| Start date | 15 August 2022 |
| Primary completion | 15 May 2023 |
| Estimated completion | 22 May 2023 |
| Sites | 3 locations across United States |
Drugs / interventions tested
- Nutritears®
- Placebo
Conditions studied
- Dry Eye — all drugs for Dry Eye →
- Dry Eye Syndromes — all drugs for Dry Eye Syndromes →
Sponsor
Applied Science & Performance Institute — full company profile →
Who can join
Adults 18 to 65, any sex, with Dry Eye or Dry Eye Syndromes. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a prospective, randomized, double-blind, parallel, placebo-controlled, clinical interventional study. The purpose of this study is to evaluate the efficacy and safety of Nutritears®, a dietary supplement of OmniActive Health Technologies, in adult subjects with dry eye syndrome (DES). Subjects shall be instructed to consume one capsule of their assigned investigational study product every morning after the breakfast, at the same time every day, for 56 days (8 weeks).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
A novel multi-ingredient supplement significantly improves ocular symptom severity and tear production in patients with dry eye disease: results from a randomized, placebo-controlled clinical trial.
Gioia N, Gerson J, Ryan R, Barbour K, et al · · 2024 · cited 2× · PMID 38984118 · DOI 10.3389/fopht.2024.1362113
Verify or expand the search:
- PubMed search for NCT05481450
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
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Currently open trials in the same condition.
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Other Applied Science & Performance Institute trials
Trials by the same sponsor.
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- NCT07225608 — The Acute Effects of Liquid IV's Pre-Workout Supplement on Muscle Endurance & Strength, Energy, and Cognition · NA · completed
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT05481450 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Applied Science & Performance Institute
- Last refreshed: 26 May 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05481450.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing