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The study of the mechanism of selective serotonin reuptake inhibitor inducing dry eye

The study of the mechanism of selective serotonin reuptake inhibitor inducing dry eye

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015592
Enrollment
Unknown
Registered
2018-04-10
Start date
2018-04-03
Completion date
Unknown
Last updated
2018-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dry eye

Interventions

SSRI:SSRI treatment
control:Psychotherapy

Sponsors

The Eye & ENT Hospital of Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Voluntarily participated in this clinical study and signed an informed consent; 2. Male or female, aged 18 to 70 years old; 3. Patients diagnosed with mild depression; 4. Patients with dry eye signs and symptoms, consistent with either criterion as follows: (1) Criterion 1: Patients with at least one positive symptom, such as dry eye, foreign body sensation, burning sensation, eye fatigue,eye distension, vision fluctuation; And tear film break-up time equal to or less than 5 seconds, or Schirmer test (without anesthetic) equal to or less than 5 mm/5 minutes; (2) Criterion 2: Patients with at least one positive symptom, such as dry eye, foreign body sensation, burning sensation, eye fatigue, eye distension, vision fluctuation; And tear film break-up time equal to or less than 10 seconds and longer than 5 seconds, or Schirmer test (without anesthetic) equal to or less than 10 mm/5 minutes and longer than 5 mm/5 minutes; And patients should show positive corneal fluorescein staining; 5. welling to follow the requirements of this study; 6. Subjects did not participate in other clinical trials during the last four weeks; 7. Subjects did not use any medications other than SSRI

Exclusion criteria

Exclusion criteria: 1. Patients with moderate or severe depression; 2. Patients with severe primary disease such as severe heart, brain and blood vessels, liver, kidney and hematopoietic systems disease; 3. Patients who received intraocular surgery or with intraocular trauma in the last six months; 4. Pregnant women and menopause women; 5. Subjects did not use any topical medications other than artifical tears, or have used these medications, but withdrawed them more than two weeks before; 6. Patients who cannot obey the required treatments and follow-ups during the trial.

Design outcomes

Primary

MeasureTime frame
Schirmer I test;Break-up Time;Ocular surface disease index (OSDI);cornea andconjunctiva stainning;MGD grading;anterior segment evaluation;Self-rating depression scale,SDS;

Countries

China

Contacts

Public ContactGong Lan

The Eye & ENT Hospital of Fudan University

13501798683@139.com+86 13501798683

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 22, 2026