NCT00386438

Brief Summary

-Does Honan balloon reduce intraocular pressure preoperatively?

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Timeline
Completed

Started Dec 2005

Shorter than P25 for phase_4

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2005

Completed
7 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2006

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

October 10, 2006

Completed
1 day until next milestone

First Posted

Study publicly available on registry

October 11, 2006

Completed
Last Updated

October 11, 2006

Status Verified

October 1, 2006

First QC Date

October 10, 2006

Last Update Submit

October 10, 2006

Conditions

Cataract

Outcome Measures

Primary Outcomes (1)

  • intraocular pressure reduction

Secondary Outcomes (1)

  • pain score

Interventions

Honan balloon applicationPROCEDURE

Eligibility Criteria

Age0 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • cataract patient,who plan to undergo phacoemulsification
  • no previous ocular surgery

You may not qualify if:

  • one eye
  • high myopia
  • Use ASA or anticoagulants
  • History of glaucoma or ocular hypertension
  • uncooperative patients

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

King Chulalongkorn Memorial hospital

Patumwan, Bangkok, 10330, Thailand

Location

Related Links

MeSH Terms

Conditions

Cataract

Condition Hierarchy (Ancestors)

Lens DiseasesEye Diseases

Study Officials

  • Thitima Lunchakonsiripan, MD

    Chulalongkorn University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
phase 4
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

October 10, 2006

First Posted

October 11, 2006

Study Start

December 1, 2005

Study Completion

July 1, 2006

Last Updated

October 11, 2006

Record last verified: 2006-10

Locations

TH(1)