Efficacy of Honan Balloon in Intraocular Pressure Reduction Before Phacoemulsification

This study has been completed.

Sponsored by:	Chulalongkorn University
Information provided by:	Chulalongkorn University
ClinicalTrials.gov Identifier:	NCT00386438

Purpose

-Does Honan balloon reduce intraocular pressure preoperatively?

Condition	Intervention	Phase
Cataract	Procedure: Honan balloon application	Phase IV

MedlinePlus related topics: Cataract

Study Type:	Interventional
Study Design:	Treatment, Randomized, Open Label, Placebo Control, Parallel Assignment, Efficacy Study

Further study details as provided by Chulalongkorn University:

Primary Outcome Measures:

Secondary Outcome Measures:

Study Start Date:	December 2005
Estimated Study Completion Date:	July 2006

Detailed Description:

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

Eligibility

Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

Exclusion Criteria:

Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00386438

Locations

Thailand, Bangkok
King Chulalongkorn Memorial hospital
Patumwan, Bangkok, Thailand, 10330

Sponsors and Collaborators

Chulalongkorn University

Investigators

Principal Investigator:

Thitima Lunchakonsiripan, MD

Chulalongkorn University

More Information

Faculty of Medicine,Chulalongkorn University This link exits the ClinicalTrials.gov site

Study ID Numbers:	391/47
Study First Received:	October 10, 2006
Last Updated:	October 10, 2006
ClinicalTrials.gov Identifier:	NCT00386438
Health Authority:	Thailand: Ethical Committee

Study placed in the following topic categories:

Eye Diseases
Cataract
Lens Diseases

ClinicalTrials.gov processed this record on January 16, 2009