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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05738629
Other study ID # 2022-0290
Secondary ID
Status Not yet recruiting
Phase Phase 1/Phase 2
First received
Last updated
Start date March 2023
Est. completion date February 2025

Study information

Verified date February 2023
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Qi Gao, Doc.
Phone 86-15088774002
Email gaoqi8977@zju.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the preliminary safety and effectiveness of Pluripotent Stem Cell-derived Mesenchymal Stem Cell Exosome (PSC-MSC-Exo) Eye Drops in the treatment of dry eye diseases post refractive surgery and associated with blepharospasm


Description:

Dry eye disease (DED) is a multifactorial disease of the ocular surface characterized by instability of the tear film and the prevalence has been estimated to reach 20%-40%. Especially, dry eye symptoms are common complaints of patients with blepharospasm or refractive surgery history, seriously affecting their quality of life. There are many conventional therapies for DED which include ocular lubricants, oral essential fatty acid supplementation, lid hygiene and warm compresses, punctal occlusion, various treatments to obstructed meibomian glands, topical antibiotics, topical corticosteroids, topical secretagogues, topical non-glucocorticoid immunomodulatory drugs and scleral contact lenses. However, the overall efficacy is still unsatisfactory with apparent side effects, long periods of treatment, and high-costs. Mesenchymal stem cell-derived exosomes (MSC-Exo) are 30-150nm microvesicles secreted by mesenchymal stem cells (MSCs), which can mediate the therapeutic efficacy of mesenchymal stem cells by the encapsulated proteins, miRNAs and other bioactive substances, and showed potential in the treatment of various diseases. This study aims to evaluate the preliminary safety and effectiveness of PSC-MSC-Exo in the treatment of dry eye diseases post refractive surgery and associated with blepharospasm. This is an open-label, single-arm, before-after study with 12 subjects with dry eye diseases and the history of refractive surgery or blepharospasm. There are 5 visits over the course of 12 weeks. Visit 1: Week-1 Visit 2: Week-2 Visit 3: Week-4 Visit 4: Week-8 Visit 5: Week-12


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 12
Est. completion date February 2025
Est. primary completion date February 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - clinical diagnosis of apparent dry eye symptoms by ophthalmologists. - patients experience dry eye symptoms with a definitive history of FS-LASIK or SMILE surgery, or blepharospasm, and previous application of artificial tears for more than 3 months could not relieve the dry eye symptoms. - have the following symptoms in at least one eye: dryness, burning sensation, foreign body sensation, discomfort in the ocular surface or visual fatigue; - tear secretion test (Schirmer's Test) of either eye = 10 mm / 5 min; - the corneal fluorescein staining score (FLCs) was more than 3 and less than 6. - Tear break up time (TBUT) is less than 10 seconds. Exclusion Criteria: - Those who are allergic to any component of the drug in this study; - Pregnant or nursing women; - Patients with active fungal, bacterial or viral keratitis or conjunctivitis; - have serious heart, lung, liver or kidney diseases; - Other incurable ocular diseases before the study; such as glaucoma, uveitis, retinitis pigmentosa. - Wearing contact lenses and unwilling to take off in the study; - Performed ocular surgery (including cataract surgery) in recent three months; - Enrolled in other interventional clinical studies at the same time; - Application of eye drops that might affect the clinical study in the past 24 hours; - Unable to complete the study according to the investigators' requirements; - Application of eye drops other than artificial tears. - Application of systemic medication known to reduce tear production, such as anti-anxiety drugs, antipsychotics and steroids. - Eyelids or eyelashes anomaly. - Serious systemic diseases. - Refused to sign the informed consent form to participate in the experiment.

Study Design


Intervention

Drug:
Pluripotent Stem Cell-derived Mesenchymal Stem Cell Exosome (PSC-MSC-Exo) Eye Drops
Participants will receive artificial tears for 2 weeks to get the normalized baseline, followed by PSC-MSC-Exo eye drops 0.125 ml/single eye/one time, four times a day for 12 weeks. The follow-up visit will be 12 weeks since the administration of PSC-MSC-Exo eye drops.

Locations

Country Name City State
China 2nd Affiliated Hospital, School of Medicine, Zhejiang University Hanzhou Zhejiang

Sponsors (3)

Lead Sponsor Collaborator
Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou yuansheng biotechnology Co., Ltd, Zhejiang University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Ocular Surface Disease Index (OSDI) The OSDI questionnaire contains 12 questions to measure dry eye symptoms. OSDI scores range from 0 to 100. The lower the score, the more alleviation of dry eye symptoms. Compared with the baseline, a reduction of more than 10 points indicates improvement. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Tear Secretion Test (Schirmer test) A paper strip is placed on the eye under the lower lid for a specified time period. The length of the strip wetted by the tears was measured in millimeters. A positive change from baseline indicates an improvement in each eye. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Tear Film Break-up Time Time required for dry spots to appear on the surface of the eye after blinking was measured in seconds. A positive change from baseline indicates improvement in each eye. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Ocular Surface Staining Score Damage of the ocular surface was measured by slit-lamp examination after staining with non-toxic fluorescein sodium. Corneal and conjunctival staining were graded as per the National Eye Institute (NEI) pictorial scale. The lower the score, the less signs of dry eye disease a patient exhibits. A negative change from baseline indicates an improvement in each eye. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Best Corrected Visual Acuity (BCVA) Whether exosomes affect visual acuity. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Conjunctiva Redness Score Conjunctival hyperemia was graded in each eye under slit-lamp magnification by assigning a score of 0 to 4 for each quadrant based on comparison to the Allergan Dry Eye Redness Scale with photographic reference where: 0=Normal, vessels of bulbar conjunctiva are easily observed; 1=Trace redness; 2=Mild redness; 3=Moderate redness; 4=Severe redness, and each score is associated with a reference photo. A negative change from baseline indicates an improvement in each eye. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Tear Meniscus Height The distance between the line of reflection along the top of the tear prism to the edge of the eyelid was measured in millimeters. A positive number change from baseline indicates improvement. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Corneal confocal microscopy The morphology, distribution and quantity of corneal nerve fibers were recorded by confocal image after LASIK and SMILE. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Meibomian gland expressibility scores Squeeze the central meibomian glands of the lower eyelid and assess the expressibility of the five central glands, where 0= All glands have meibum extruded, 1= 3-4 glands have meibum extruded, 2=1-2 glands have meibum extruded, 3=no glands have meibum extruded. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
Secondary Meibomian Glands Photography The morphology, quantity and blockage of meibomian gland can be assigned a score of 0 to 3 points according to meibomian gland dropout, where 0=normal without dropout; 1=meibomian gland dropout<1/3; 2=meibomian gland dropout 1/3-2/3; 3=meibomian gland dropout >2/3. The total score of upper and lower meibomian glands is 6 points, of which Grade 0=0-1 point; Grade 1=2-3 points; Grade 2=4-5 points; Grade 3=6 points. 1 weeks, 2 weeks, 4 weeks, 8 weeks,12 weeks
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