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Clinical Trials/ISRCTN66846344
ISRCTN66846344
Completed
Not Applicable

A pilot randomised controlled trial comparing the post-operative pain experience following vitrectomy with a 20-gauge system and the new 25-gauge transconjunctival system

Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)0 sites50 target enrollmentSeptember 30, 2005
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Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)
Enrollment
50
Status
Completed
Last Updated
11 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 30, 2005
End Date
TBD
Last Updated
11 years ago
Study Type
Interventional

Investigators

Sponsor
Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)

Eligibility Criteria

Inclusion Criteria

  • •Added April 2008:
  • •1\. Patients with suitable pathology for the 25 gauge system eg macula hole, epiretinal membrane, vitreous opacities
  • •2\. Primary vitrectomy

Exclusion Criteria

  • •Added April 2008:
  • •1\. Previous vitrectomy
  • •2\. Unwilling to accept randomisation
  • •3\. Unable to give informed consent
  • •4\. Pre\-operative inflammation

Outcomes

Primary Outcomes

Not specified

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