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Efficacy and Safety of A New Eye Massager Device in Treatment for Dry Eye Disease

Efficacy and Safety of A New Eye Massager Device in Treatment for Dry Eye Disease

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025047
Enrollment
Unknown
Registered
2019-08-09
Start date
2017-06-01
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Dry eye disease

Interventions

Group 1:Eye massager treatment
Group 2:Artificial tears treatment

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) with a diagnosis of DED according to the criteria proposed by the Tear Film and Ocular Surface Society (TFOS) Dry Eye Workshop (DEWS); (2) who were willing to cooperate during the examination and treatment procedure, and sign the inform consent; (3) with ability to participate in follow-up examinations for at least three weeks during the treatment.

Exclusion criteria

Exclusion criteria: (1) patients with active allergies, infections, or inflammatory diseases of the ocular surface unrelated to dry eye within six months; (2) patients who used treatments for DED within the last month; (3) a history of ocular trauma or surgery within one year; (4) patients with alterations in the lacrimal drainage system such as punctal occlusion; (5) patients who used contact lenses within the past month; (6) patients with uncontrolled systemic diseases; (7) pregnant or nursing mothers.

Design outcomes

Primary

MeasureTime frame
Dry eye symptoms questionnaire;BUT;Schirmer I test;Corneal fluorescein staining;Conjunctival injection;

Countries

China

Contacts

Public ContactXuemin Li

Peking University Third Hospital

lxmlxm66@sina.com+86 13911254862

Outcome results

None listed

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