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Intra and Postoperative Outcomes With 3 Injectors

NCT02466256 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2015-06-09

No results posted yet for this study

Summary

This randomized clinical trial compares subjective performance during Intraocular lens (IOL) implantation, as well as incision enlargement and anterior segment morphology on OCT when IOL implantation was performed during microcoaxial phacoemulsification through a 2.2mm incision using one of three injectors :

Manual screw type (Monarch III), Manual plunger type (Royale) and motorised injector (Autosert). Further, the investigators also looked at incision integrity by comparing ingress of trypan blue from the ocular surface into the anterior chamber.

Conditions

  • Cataract

Interventions

PROCEDURE

Intraocular lens implantation

Intraocular lens implantation

DEVICE

Autosert Injector

Motorised injection device for intraocular lens implantation

DEVICE

Royale Injector

Manual, plunger type injection device for intraocular lens implantation

DEVICE

Monarch III Injector

Manual, screw type injection device for intraocular lens implantation

Sponsors & Collaborators

  • Iladevi Cataract and IOL Research Center

    lead OTHER

Principal Investigators

  • abhay r vasavada, ms, frcs · iladevi cataract & iol research centre

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
SINGLE_GROUP

Eligibility

Min Age
40 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-12-31
Primary Completion
2014-06-30
Completion
2014-06-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02466256 on ClinicalTrials.gov