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Clinical visual outcome of multifocal intraocular lens

Clinical visual outcome of multifocal intraocular lens

Status
Unknown
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20241115002
Enrollment
15
Registered
2024-11-15
Start date
2024-04-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Cataract Intraocular lens Multifocal monofocal cataract

Interventions

patient with intraocular lens (Acriva trinova pro C)
Treatment

Sponsors

None listed

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. age more than 50 years 2. A person who comes for an eye exam at the eye department has been diagnosed with cataracts in both eyes and wants to wear artificial lenses that can see at multiple distances.

Exclusion criteria

Exclusion criteria: 1. People with a history of eye disease other than cataracts or have had any other type of eye surgery before 2. Calculation of intraocular lens power (IOL power) using the IOLMaster 700 with corneal astigmatism greater than 0.75 diopter. 3. Patients unable to undergo various examination procedures

Design outcomes

Primary

MeasureTime frame
Uncorrected visual acuity 1 week, 1 month, 3 months Logarithm of the Minimum Angle of Resolution / at 30 cm, 60 cm and distance

Secondary

MeasureTime frame
Rates of glare/halo complaints 1 week, 1 month, 3 months percentage

Countries

Thailand

Contacts

Public ContactNiphon Chirapapaisan

Faculty of Medicine Siriraj Hospital, Mahidol University, Mahidol University

niphon.chi@mahidol.ac.th0896685735

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026