Limbal Stem Cell Derived Exosome (LSC-Exo) Eye Drop for Treatment of Dry Eye
NCT06543667 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2025-05-01
Summary
The purpose of this study is to determine the safety and efficacy of Limbal Stem Cells derived Exosomes (LSC-Exo) in alleviation of dry eye symptoms
Conditions
- Dry Eye Syndromes
Interventions
- BIOLOGICAL
-
Limbal Stem Cell Derived Exosomes Eye Drop
Patients will receive artificial tears for 2 weeks to get the normalized baseline, followed by LSC-Exo eye drops 0.15 ml/single eye/one time, four times a day for 3 months. The follow-up visit will be 12 weeks since the administration of LSC-Exo eye drops.
Sponsors & Collaborators
-
Iran University of Medical Sciences
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-01
- Primary Completion
- 2026-01-01
- Completion
- 2026-07-01
Countries
- Iran
Study Locations
More Related Trials
-
Exosomes in Patients With Ocular Involvement of Sjögren's Syndrome
NCT07192666 ·Status: NOT_YET_RECRUITING ·Phase: EARLY_PHASE1
-
Therapeutic Effect of Stem Cell Eye Drops on Dry Eye Disease
NCT05784519 ·Status: ACTIVE_NOT_RECRUITING ·Phase: EARLY_PHASE1
-
A Clinical Study to Assess the Safety and Efficacy of an Ophthalmic Solution (SkQ1) in the Treatment of Dry Eye Syndrome (DES)
NCT02121301 ·Status: COMPLETED ·Phase: PHASE2
-
Safety and Efficacy Study of Iontophoresis and Dexamethasone Phosphate to Treat Dry Eye
NCT00765804 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Determine the Safety and Tolerability of Escalating Doses of INS365 Ophthalmic Solution
NCT00680108 ·Status: COMPLETED ·Phase: PHASE2
-
Probiotic in Dry Eye Syndromes
NCT04938908 ·Status: COMPLETED ·Phase: PHASE2
-
A Study of INS365 Ophthalmic Solution in Patients With Moderate to Severe Dry Eye Disease
NCT00679718 ·Status: COMPLETED ·Phase: PHASE2
-
Effects of 3% Diquafosol on Tear Film and Vision-related Quality of Life in Orthokeratology Lens Related Dry Eye
NCT06537349 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Clinical Trial to Evaluate the Safety and Efficacy of SCAI-001 Compared to Restasis
NCT05733624 ·Status: COMPLETED ·Phase: PHASE2
-
Study of INS365 Ophthalmic Solution in Subjects With Dry Eye Disease
NCT00404131 ·Status: COMPLETED ·Phase: PHASE3
-
Platelet -Rich Plasma (PRP) Injection for the Treatment of Severe Dry Eye
NCT02257957 ·Status: COMPLETED ·Phase: PHASE3
-
Corneal Epithelial Stem Cells and Dry Eye Disease
NCT03302273 ·Status: COMPLETED ·Phase: NA
-
Efficacy and Safety Study of TJCS for Treatment of Moderate to Severe Dry Eye Syndromes
NCT02461719 ·Status: COMPLETED ·Phase: PHASE3
-
Study of INS365 Ophthalmic Solution in Subjects With Dry Eye Disease
NCT00403715 ·Status: COMPLETED ·Phase: PHASE3
-
Study of SkQ1 as Treatment for Dry-eye Syndrome
NCT03764735 ·Status: COMPLETED ·Phase: PHASE3
-
A Dose-Escalation Study to Assess the Safety and Tolerability of LX214 Ophthalmic Solution in Healthy Volunteers, Followed by an Open-Label Evaluation of LX214 in Patients With Keratoconjunctivitis Sicca (KCS)
NCT00851734 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy of Platelet-Rich Plasma Injection in Dry Eye Syndrome
NCT06831253 ·Status: RECRUITING ·Phase: NA
-
Evaluating the Efficacy and Safety of TJO-087 in Moderate to Severe Dry Eye Disease Patients
NCT05245604 ·Status: UNKNOWN ·Phase: PHASE3
-
Safety and Efficacy of Licaminlimab Ophthalmic Solution for the Treatment of Dry Eye Disease
NCT05896670 ·Status: COMPLETED ·Phase: PHASE2
-
The Effects of a Single Intravenous Administration of Secukinumab (AIN457) or Canakinumab (ACZ885) in Dry Eye Patients
NCT01250171 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Tolerability, Plug Retention and Preliminary Efficacy of Tacrolimus-loaded Punctal Plug in Patients With Moderate to Severe Dry Eye Disease - Cohort B
NCT05618730 ·Status: UNKNOWN ·Phase: PHASE1
-
Ditefossol Sodium 3% Eye Drops in Patients With Dry Eye
NCT06560580 ·Status: COMPLETED ·Phase: NA
-
Use of 3% Diquafosol Topical Ophthalmic Solution for Diabetic Dry Eye
NCT05193331 ·Status: UNKNOWN ·Phase: NA
-
A Study Evaluating the Efficacy and Safety of RCI001 Ophthalmic Solution Compared to Placebo in Subjects With Dry Eye
NCT07068958 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Vehicle-Controlled Study of SkQ1 as Treatment for Dry-eye Syndrome
NCT04206020 ·Status: COMPLETED ·Phase: PHASE3