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Clinical study on prostaglandin associated periorbitopathy

Clinical study on prostaglandin associated periorbitopathy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045465
Enrollment
Unknown
Registered
2021-04-15
Start date
2019-11-29
Completion date
Unknown
Last updated
2021-11-29

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

Conditions

Glaucoma

Interventions

bimatoprost group:Use bimatoprost
travoprost group:Use travoprost
latanprost group:Use latanprost
tafluprost group:Use tafluprost

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1.Those who meet the diagnostic criteria of POAG or ocular hypertension in China; 2.Those who had never used prostaglandins had the latter after the elution period of other drugs.

Exclusion criteria

Exclusion criteria: 1.Previous eye surgery (except for cataract superemulsification) and eye trauma; 2.Chronic eye diseases (blepharoptosis, thyroid-related eye diseases, orbital tumors and other diseases that cause ocular protrusion or depression); 3.Wearing contact lenses; 4.Patients with unsuitable general conditions: for example, patients with bronchial asthma, patients with severe chronic obstructive pulmonary disease, bradycardia, patients with II or III degree atrioventricular block, patients with obvious heart failure and cardiogenic shock should not use ß-blockers, as well as patients with allergies to the selected drugs.

Design outcomes

Primary

MeasureTime frame
pupil distance;degree of exophthalmus;margin reflex distance;

Countries

China

Contacts

Public ContactNi Li

West China Hospital of Sichuan University

linidoc@163.com+86 18980605779

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026