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The effect of eyepoint for early dryeye and patient satisfaction after small incision lenticule extraction

The effect of eyepoint for early dryeye and patient satisfaction after small incision lenticule extraction

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16010074
Enrollment
Unknown
Registered
2016-12-02
Start date
2016-09-21
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

early dry eye after SMILE

Interventions

experimental group:eyepoint with artificial tears

Sponsors

Shanghai Research Institute of Acupuncture and Meridian
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patient who suffer dry eye after SMILE; (2) Aged 18 to 40 years old; (3) Preoperative concave-sphere -3.0 to -10.0DS.Preoperative concave-cylinder:0 to 5.0DC; (4) Patient who didn't suffer dry eye before operation; (5) Patient with good compliance who volunteers to join the subject and signs informed consent.

Exclusion criteria

Exclusion criteria: (1) Patient who use any ocular surface medicine before examination on the day; (2) Patient who suffered external eye disease or took operation of external eye in 6 months; (3) Patient who took permanent or temporary smart plug in half year before this operation; (4) Patient who is suffering else eye disease; (5) Patient who use other oral medicine or external medicine which treat eye disease at the same time; (6) Patient who is in gestation period or lactation; (7) Patient who has cardiovascular, cerebrovascular, hepatic, renal, hematopoietic systematic diseases or other systematic disease and mental disease.

Design outcomes

Primary

MeasureTime frame
tear film break-up time;Schimer I test;corneal sensitivity;tear meniscus height;

Countries

China

Contacts

Public ContactXiaopeng Ma

Shanghai Research Institute of Acupuncture and Meridian

pengpengma@163.com+86 13917140446

Outcome results

None listed

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