Study of Platelet Rich Plasma Drops to Moderate Clinically Significant Dry Eye

NCT05121493 | Not Yet Recruiting

• 1 other identifier: STUDY00004552
• Study Type: interventional
• Target: 15
• Locations: 1 country
• Sites: 1

Brief Summary

This is a single center double-masked study with up to four visits. Subjects who have been diagnosed with dry-eye syndrome at Flaum Eye Institute will be enrolled. The purpose of the study is to determine if using platelet rich plasma drops can improve clinically significant dry eye in patients and determine if there is a difference with using two different uses of the plasma tear drops: platelet rich plasma tears and plasma tears without platelets.

Conditions

Dry Eye Syndromes

Outcome Measures

Primary Outcomes (5)

• Mean change in acuity

  Acuity will be measured using a Shack-Hartmann Wavefront Sensor. Subjects will be seated in front of the wavefront sensor. They will be asked to blink naturally fixate on the laser spot throughout the measurement protocol. While subjects fixate, the wavefront sensor delivers a brief flash of light to the subjects' retina. The light reflected out of the subjects' eye is collected to obtain measurements of wavefront aberrations of the eye. For optical quality assessments the measurements of wavefront aberrations will be acquired along the line-of-sight. The wavefront data acquired from the wavefront sensor will be described by Zernike coefficients, the most popular mathematical way to represent the ocular aberrations.

  baseline to 3 months

• Mean change in breakup pattern to appear

  This will be measured using a Placido Disk. The subject places their chin on a chin rest and look into the disk system. The system uses an incandescent or broad-band area LED for illumination.

  baseline to 3 months

• Mean change in lipid coverage of the cornea with blinking

  This will be measured using a Ellipsometer/Tearscope. This instrument uses a modified slit-lamp head restraint and an imaging system to visualize the surface of the subject's cornea. Structurally the system is a clinical slit-lamp system. However, the system uses an electronic camera instead of a human observer. The illumination system uses a diffuse ring illuminator instead of a slit-lamp. The data from this instrument identifies changes in the lipid thickness and the refractive index over the cornea.

  baseline to 3 months

• Mean change in consistency of lipid compensation

  This will be measured using a Ellipsometer/Tearscope. This instrument uses a modified slit-lamp head restraint and an imaging system to visualize the surface of the subject's cornea. Structurally the system is a clinical slit-lamp system. However, the system uses an electronic camera instead of a human observer. The illumination system uses a diffuse ring illuminator instead of a slit-lamp. The data from this instrument identifies changes in the lipid thickness and the refractive index over the cornea.

  baseline to 3 months

• Mean change in temperature over the optical service

  This will be measured using a Thermal Imaging System. A thermal imaging system will be used to provide spatially-resolved thermal maps of the subject's eyes and face adjacent to the eyes. This camera system is non-invasive and is mounted on a tripod about 12" from the subject's eyes. It images the heat that is emitted by the subject at frame rates from 2 to 10 Hz. The camera displays a spatially resolved map (approximately 0.2 x 0.2 mm pixel size) of the ocular surface temperature. IR detection is a convenient tool for instantaneous temperature measurement of the ocular surface and allows monitoring of time course change as well.

  baseline to 3 months

Study Arms (2)

Platelet Poor Plasma Tear

ACTIVE COMPARATOR

Other: Platelet Poor Plasma Tear Drops

Platelet Rich Plasma Tears

EXPERIMENTAL

Other: Platelet Rich Plasma Tear Drops

Interventions

Platelet Poor Plasma Tear Drops OTHER

Participant blood will be drawn and processed by the University of Rochester Transfusion Medicine and Blood Bank. Processing will isolate the platelet free fraction of the blood plasma. After processing, plasma should contain ≤ 5% concentration of white blood cells (WBC), red blood cells (RBC), and platelets when compared to the concentration before processing.

Platelet Poor Plasma Tear

Platelet Rich Plasma Tear Drops OTHER

Participant blood will be drawn and processed by the University of Rochester Transfusion Medicine and Blood Bank. Processing will isolate the platelet fraction of the blood plasma. After processing, plasma should contain ≤ 5% concentration of WBC and RBC and 100 x 10³ μl or ≥ 50% recovery of platelets when compared to the pre-platelet count.

Platelet Rich Plasma Tears

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Subjects must be diagnosed with clinically significant dry eye.
• Subjects have no active ocular disease or allergic conjunctivitis.
• Subjects must not be using any topical ocular medications within two weeks prior to enrollment.
• Subjects must be willing and able to follow instructions.
• Subjects must have voluntarily agreed to participate in the study by signing the statement of informed consent.
• Subjects must meet plasma donor criteria as established by University of Rochester Transfusion Medicine \& Blood Bank.

You may not qualify if:

• Is pregnant at the time of enrolment in the study determined by urine pregnancy test.
• Is currently on a course of antibiotics
• Is considered by the Investigator to not be a suitable candidate for participation and are not at risk for glaucoma.
• Is considered by the University of Rochester Transfusion Medicine \& Blood Bank not a suitable candidate for blood donation.

Sponsors & Collaborators

• University of Rochester: lead

Study Sites (1)

Flaum Eye Institute at the University of Rochester

Rochester, New York, 14642, United States

Location

MeSH Terms

Conditions

Dry Eye Syndromes

Condition Hierarchy (Ancestors)

Lacrimal Apparatus Diseases; Eye Diseases

Central Study Contacts

James Aquavella, MD

CONTACT

585-273-3937; james_aquavella@urmc.rochester.edu

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Professor

Study Record Dates

• First Submitted: November 3, 2021
• First Posted: November 16, 2021
• Study Start: October 15, 2025
• Primary Completion (Estimated): December 15, 2026
• Study Completion (Estimated): December 15, 2026
• Last Updated: November 26, 2024

Record last verified: 2024-07

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)