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Relationship Between Topiramate Use and Ocular Angle Status

Relationship Between Topiramate Use and Ocular Angle Status: A Prospective Pilot Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00153699
Enrollment
15
Registered
2005-09-12
Start date
2004-09-30
Completion date
2007-07-31
Last updated
2007-10-31

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

Conditions

Glaucoma, Angle-Closure

Keywords

Side effects, Topiramate

Brief summary

We test the hypothesis whether topiramate narrows the angles which may render Asians more likely to suffer from acute angle closure glaucoma.

Detailed description

Topiramate is approved for the treatment of epilepsy and prophylaxis of migraine attacks. There were case reports of acute angle closure glaucoma (AACG) associated with its use. AACG is particularly common in Asians because of a higher prevalence of narrow angle., we test the hypothesis whether topiramate narrows the angles which may render them more likely to suffer from AACG.

Interventions

DRUGTopiramate

Sponsors

Hong Kong Eye Hospital
CollaboratorOTHER
Chinese University of Hong Kong
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Participants aged 18-75 with an indication for starting topiramate.

Exclusion criteria

* Patients with known allergy or intolerance to topiramate. * Recent exposure to topiramate (\<3 months). * Moderate to severe renal failure. * Known history of renal calculi or hepatic failure * Inability to give informed consent. * Pregnant women or women of child-bearing age who do not practise an acceptable means of contraception. * Patients known to have angle-closure glaucoma.

Design outcomes

Primary

MeasureTime frame
Change(s) in ophthalmic parameters measured at baseline and after 4 weeks of treatment, including:4 weeks
best-corrected visual acuity, refraction, Goldmann applanation tonometry, Gonioscopy, dilated fundus examination,4 weeks
and ultrasound biomicroscopy of angle and anterior segment.4 weeks

Countries

Hong Kong

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026