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a clinical case controled trial for the intraocular tamponade in the vitrectomy for rhegmatogenous retinal detachment(RRD).

a clinical case controled trial for the intraocular tamponade in the vitrectomy for rhegmatogenous retinal detachment(RRD). - RRD tamponade study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006993
Enrollment
50
Registered
2012-01-01
Start date
2012-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Rhegmatogenous retinal detachment

Interventions

We replace vitreous with air at the end of surgery. The air tamponade will disappear applex 7 days. We replace vitreous with SF6 at the end of surgery. The air tamponade will disappear applex 14 days

Sponsors

Department of ophthalmology,Kansai medical university
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The RRD patients who consulted this hospital and meet following criterion. .A clinical record at the time of study entry contains no definiency for essential points. .20 yearsold or older. .The affected eye caan be evaluated of the retinal tear at the upper of retina and the RRD is not old RRD. .The affected eye shuld have no other clinically significant abnormality which may cause loss of vision. .The affected eye does noy have the record of votreous surgery. .The eye length oh affected eye is not 26mm or over 26mm.

Exclusion criteria

Exclusion criteria: .When the patient does not hope for entry. .In the case when there is a unsuspected worsening of the disease or advance event which the patient should exist this study.

Design outcomes

Primary

MeasureTime frame
we try to compare the improvement of the retio of reattachment and BCVA after vitrectomy at the point of 1.3.6.12 months postoperatively.

Countries

Japan

Contacts

Public ContactToshimitsu Ishiguro

Kansai medical university Hirakata hospital

0728040101

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026