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OpenTrials
Completed

NCT Number: NCT00386438

Efficacy of Honan Balloon in Intraocular Pressure Reduction Before Phacoemulsification

-Does Honan balloon reduce intraocular pressure preoperatively?

Completed

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Key information

Conditions

Cataract Eye Diseases Lens Diseases

Age range

0 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

King Chulalongkorn Memorial hospital

Patumwan, Bangkok, 10330, Thailand

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Honan balloon application

Procedure

Primary outcomes

  1. intraocular pressure reduction

Secondary outcomes

  1. pain score

Sponsors and collaborators

Lead sponsor

Chulalongkorn University

Other

Registry information

Important dates

Study start
2005
Study completion
2006
First posted
Oct 11, 2006
Registry last updated
Oct 11, 2006

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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