Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT03068377 · ClinicalTrials.gov registry record · NA

The Effects of LycoRed Phytonutrient and Vitamin Supplement (a.k.a. LYC-001e) on Ocular Blood Flow

A NA study of Ocular Blood Flow, sponsored by LycoRed.

Completed
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT03068377: Completed NA study of Ocular Blood Flow, sponsored by LycoRed.

NCT03068377 is a NA study of Ocular Blood Flow that has completed, run by LycoRed. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03068377, a NA study of Ocular Blood Flow, has completed, sponsored by LycoRed.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

Objectives:To determine LYC-001e's influences on ocular blood flow Ocular blood flow has been implicated as a parameter relevant to eye health and involved in the disease process of several ophthalmic pathologies including AMD, glaucoma, and diabetes We hypothesis that LYC-001e will increase measures of ocular blood flow in healthy individuals Methods: This is a single-phase, randomized, parallel, double blind , comparative study of LYC-001e versus placebo on ocular blood vessels in healthy individuals.

Primary Outcome

Measures retinal capillary blood flow

Conditions Studied

Interventions

  • DIETARY_SUPPLEMENT Placebo
  • DIETARY_SUPPLEMENT Experimental

Study Locations (1)

Indiana

  • Glaucoma Research and Diagnostic Center Eugene and Marilyn Glick Eye Institute Indiana University School of Medicine - Indianapolis

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2017-03-20
Est. Completion 2018-12-30
Phase NA
LycoRed

7 total trials

What the finished NCT03068377 record still lists

NCT03068377 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 1 condition, with Ocular Blood Flow appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT03068377 reports a single indexed study location in Indiana.

Frequently Asked Questions

What is clinical trial NCT03068377 about?

NCT03068377 is a clinical study titled "The Effects of LycoRed Phytonutrient and Vitamin Supplement (a.k.a. LYC-001e) on Ocular Blood Flow". Objectives:To determine LYC-001e's influences on ocular blood flow Ocular blood flow has been implicated as a parameter relevant to eye health and involved in the disease process of several ophthalmic pathologies including AMD, glaucoma, and diabetes We hypothesis that LYC-001e will increase measure...

What is the current status of trial NCT03068377?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2017-03-20. Estimated completion is 2018-12-30.

What conditions does trial NCT03068377 study?

This clinical trial studies the following conditions: Ocular Blood Flow.

What interventions are being tested in trial NCT03068377?

The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Experimental (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT03068377?

This trial is sponsored by LycoRed, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT03068377 being conducted?

This trial has 1 study location across Indiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

How this trial's enrollment target compares

Where NCT03068377's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT03068377, the US trial registry maintained by the National Library of Medicine. NCT03068377 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.