Analysis of the effect of bandage contact lens used on ocular biological measurements and intraocular lens power calculations

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100041902

Enrollment

Unknown

Registered

2021-01-09

Start date

2021-01-15

Completion date

Unknown

Last updated

2021-03-30

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

Conditions

ocular surface disease

Interventions

A:Wear a bandage type contact lens with a base arc of 8.4mm

B:Wear a bandage type contact lens with a base arc of 8.6mm

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: 1. Healthy volunteers aged 20-40 years; 2. Fluorescein stained tear film burst time BUT >= 5'.

Exclusion criteria

Exclusion criteria: 1. Eye diseases; 2. A history of eye surgery: including laser surgery for myopia, etc.; 3. Wear soft contact lenses in the past 2 weeks and hard contact lenses in the past 1 month; 4. Patients with dry eye/MGD; 5. Obviously unsuitable for wearing corneal bandage lens in the past;

Design outcomes

Primary

Measure	Time frame
Ocular surface biological parameters;Intraocular lens power;	—

Countries

China

Contacts

Public ContactDing Chen

Eye Hospital and School of Ophthalmology and Optometry, Wenzhou Medical University

necoding@126.com+86 13867702411

Outcome results

None listed

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