Efficacy of Honan Balloon in Intraocular Pressure Reduction Before Phacoemulsification

This study has been completed.
Sponsor:
Information provided by:
Chulalongkorn University
ClinicalTrials.gov Identifier:
NCT00386438
First received: October 10, 2006
Last updated: NA
Last verified: October 2006
History: No changes posted
  Purpose

-Does Honan balloon reduce intraocular pressure preoperatively?


Condition Intervention Phase
Cataract
Procedure: Honan balloon application
Phase 4

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

Resource links provided by NLM:


Further study details as provided by Chulalongkorn University:

Primary Outcome Measures:
  • intraocular pressure reduction

Secondary Outcome Measures:
  • pain score

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:

  • 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
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

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

Locations
Thailand
King Chulalongkorn Memorial hospital
Patumwan, Bangkok, Thailand, 10330
Sponsors and Collaborators
Chulalongkorn University
Investigators
Principal Investigator: Thitima Lunchakonsiripan, MD Chulalongkorn University
  More Information

Additional Information:
No publications provided

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

Additional relevant MeSH terms:
Cataract
Lens Diseases
Eye Diseases

ClinicalTrials.gov processed this record on July 20, 2014