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The effect on blink frequency of a selective blue-filtering photochromic lens in patients with benign essential blepharospasm

The effect on blink frequency of a selective blue-filtering photochromic lens in patients with benign essential blepharospasm - blue-filtering lens in BEB

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032135
Enrollment
30
Registered
2023-07-03
Start date
2014-09-08
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

G24.5

Interventions

Group 1: photo-protective and photo-selective blue-filtering ophthalmic lenses for two weeks Group 2: Placebo ophthalmic lenses for two weeks

Sponsors

Medizinische Universität Wien
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: idiopathic benign essential blepharospasm

Exclusion criteria

Exclusion criteria: any other disease with involuntary blinking (Hemifacial spasm, Tic disorder, Tardive dyskinesia, etc.); in case of ongoing BoNT therapy < 12 weeks since last BoNT injection, acute or chronic severe medical conditions which would preclude the subject from participating; a medical history of dementia or seizure disorder; pregnancy; less than 18 years old; unable or unwilling to give informed consent/ to cooperate with study requirements.

Design outcomes

Primary

MeasureTime frame
Change in blink frequency - Comparison of baseline to 2 weeks after verum glasses and 2 weeks after placebo glasses

Secondary

MeasureTime frame
blink frequency under different conditions: Resting condition (looking straight ahead) – 3 minutes Reading a standardized text – 3 minutes Playing a monitor interactive game – 3 minutes 3 different photopic conditions (99%, 64%, 33% contrast) - each 6 minutes

Countries

Austria

Contacts

Public ContactThomas Sycha

Medizinische Universität Wien

thomas.sycha@meduniwien.ac.at+43-1-40400-31450

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 7, 2026