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Effect observation on application of evidence-based care plan of patients with demodex related dry eye diseases

Effect observation on application of evidence-based care plan of patients with demodex related dry eye diseases

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080129
Enrollment
Unknown
Registered
2024-01-22
Start date
2023-03-01
Completion date
Unknown
Last updated
2024-01-28

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

Conditions

demodex related dry eye diseases

Interventions

The control group:Provide the routine care.
The observation group:Privide the evidence-based care plan.

Sponsors

Shanghai Genneral Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1) Diagnosed with demodex associated dry eye; 2) At least 18 years of age; 3) Informed consent of the patient or his family.

Exclusion criteria

Exclusion criteria: 1) Patients who have received anti-mite treatment; 2) Patients who have undergone eye surgery; 3) Patients with allergies; 4) Patients who voluntarily quit and those who do not sign the informed consent; 5) Other reasons that the researcher considers unsuitable for inclusion in the project; 6) Participants identified by the researcher as unfit to continue to participate in the experiment during the study.

Design outcomes

Primary

MeasureTime frame
The number of demodex mites;Tear secretion test (Schirmer ? test) results;Results of Chinese Dry Eye Questionnaire;Corneal fluorescence staining results;fluorescein breakup time (FBUT);

Secondary

MeasureTime frame
Zung's self-rating Depression Scale;SAS self-rating Anxiety Scale.;

Countries

china

Contacts

Public ContactWenyue Dou

Shanghai Genneral Hospital

343923337@qq.com+86 137 0187 0929

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026