NCT00386438

CompletedPhase 4

Efficacy of Honan Balloon in Intraocular Pressure Reduction ...

Chulalongkorn University Source

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Other study identifiers

Sponsor study identifier

391/47

Study Type

interventional

Reported enrollment (type unavailable)

N/A

Locations

1 country

Sites

1

Timeline

Study Start

December 2005

Date type not reported

This date has not been verified as actual or estimated.

Primary Completion

Not reported

Date not reported

Study Completion

July 2006

Date type not reported

This date has not been verified as actual or estimated.

Brief Summary

-Does Honan balloon reduce intraocular pressure preoperatively?

Registry Overview

Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.

Recruitment status: completed
Reported enrollment (type unavailable): Not reported
Study completion date: July 2006
Date type not reported
This date has not been verified as actual or estimated.
Listed locations: 1 countries · 1 sites

Trial Relationships

Click on a node to explore related trials.

Some registry-reported names shown below are not yet linked in this graph.

Study Timeline

Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.

Study Start
December 2005
Date type not reported
This date has not been verified as actual or estimated.
Study Completion
July 2006
Date type not reported
This date has not been verified as actual or estimated.
First Submitted
October 10, 2006
Actual (reported)
First Posted
October 11, 2006
Actual (reported)

Last Updated: October 11, 2006
Status Verified: October 2006
Last Update Submitted: October 10, 2006

Conditions

Cataract

Outcome Measures

Primary Outcomes (1)

intraocular pressure reduction

Secondary Outcomes (1)

pain score

Interventions

Honan balloon applicationProcedure

Registry-reported names are shown in full. Names without a link have not yet been matched to a Syfrah profile.

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:

Sponsors & Collaborators

Chulalongkorn University
Otherlead

Study Sites (1)

King Chulalongkorn Memorial hospital

Patumwan, Bangkok, 10330, Thailand

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 2005

Date type not reported

This date has not been verified as actual or estimated.

Study Completion

July 2006

Date type not reported

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Phase 4Completed

NCT01028872

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Phase 4Completed

NCT00312299

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Phase 4Completed

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

Contact the study team to confirm eligibility.

This date has not been verified as actual or estimated.

Last Updated

October 11, 2006

Record last verified: 2006-10

Source record

Download the complete ClinicalTrials.gov record imported by Syfrah, including fields not shown in this page. The registry may contain a newer revision.

Source: ClinicalTrials.gov.

JSON downloads include source attribution and retrieval details alongside the unchanged original record or the separately normalized values.

Registry identifier: NCT00386438
Data provider: ClinicalTrials.gov
Source updated: 2006-10-11
Normalization version: ctgov-legacy-1

Open registry record

Source retrieved: 2026-10-25 22:23:47 UTC

Locations

TH(1)

Efficacy of Honan Balloon in Intraocular Pressure Reduction Before Phacoemulsification

Brief Summary

Registry Overview

Trial Relationships

Study Timeline

Study Start

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Study Design

Study Record Dates

Source record

Locations

Brief Summary

Registry Overview

Trial Relationships

Related Scientific Literature

Study Timeline

Study Start

Study Completion

First Submitted

First Posted

Conditions

Outcome Measures

Primary Outcomes (1)

Secondary Outcomes (1)

Interventions

Eligibility Criteria

You may qualify if:

You may not qualify if:

Sponsors & Collaborators

Study Sites (1)

Related Links

MeSH Terms

Conditions

Condition Hierarchy (Ancestors)

Study Officials

Study Design

Study Record Dates

Source record

Locations