Efficacy of Honan Balloon in Intraocular Pressure Reduction Before Phacoemulsification

Cataract Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00386438
• Other study ID #: 391/47
• Status: Completed
• Phase: Phase 4
• First received: October 10, 2006
• Last updated: October 10, 2006
• Start date: December 2005
• Est. completion date: July 2006

Study information

• Verified date: October 2006
• Source: Chulalongkorn University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Thailand: Ethical Committee
• Study type: Interventional

Clinical Trial Summary

-Does Honan balloon reduce intraocular pressure preoperatively?

Description:

-Does Honan balloon improve surgeon's satisfaction and patients' pain score when compared to no honan group?

Recruitment information / eligibility

• Status: Completed
• Enrollment: 0
• Est. completion date: July 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• cataract patient,who plan to undergo phacoemulsification

• no previous ocular surgery

Exclusion Criteria:

• one eye

• high myopia

• Use ASA or anticoagulants

• History of glaucoma or ocular hypertension

• uncooperative patients

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Cataract

Intervention

Procedure:
• Honan balloon application

Locations

Country	Name	City	State
Thailand	King Chulalongkorn Memorial hospital	Patumwan	Bangkok

Sponsors (1)

Lead Sponsor	Collaborator
Chulalongkorn University

Country where clinical trial is conducted

Thailand, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	intraocular pressure reduction
Secondary	pain score

External Links

•   Faculty of Medicine,Chulalongkorn University