asthenopia
Conditions
Interventions
experimental group:deliver compoud naphthalene to conjunctiva capsule
control group:deliver single naphthalene to conjunctiva capsule
Sponsors
Eye & ENT Hospital of Fudan University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Aged 18~65 years old male and female; 2. Symptoms of asthenopia caused by various causes, and 2 or more of the symptoms listed; 3. The total score of clinical observation indicators is at least 15; 4. Volunteered to be subject, understand and sign the informed consent.
Exclusion criteria
Exclusion criteria: 1. Having any eye disease that affected the clinical study; 2. Severe heart, lung, liver, renal dysfunction; 3. Pregnant and lactating women; 4. Psychopath; 5. Allergic to any known ingredient in the test drug and control drug; 7. Other drugs that may affect the evaluation of the results of this experiment are being applied throughout the body or part of the body.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| vision;intraocular pressure;cornea fluorescein staining;eye tolerance; | — |
Countries
China
Contacts
Public ContactXinghuai Sun
Eye & ENT Hospital, Shanghai Medical College, Fudan University
Outcome results
None listed