CompletedNot Applicable

Modification of Scleral Suture Fixation of Dislocated IOL

Sweden117 participantsStarted 2018-11-12

Plain-language summary

A prospective randomized study on patients with late in the bag intraocular lens (IOL) dislocation after cataract surgery. Two surgical techniques of suturing of IOL to the sclera will be compared in the study. IOL position will be compared between those two groups, as well to a control group consisting of ordinary pseudophakia where only measurement of IOL position will be performed.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * patients with in-the-bag dislocated IOL who agree to participate in the study * Inclusion criteria for the control group: pseudophakic eyes 7-10 years after uneventful cataract surgery. Exclusion Criteria: * patients with dislocated IOL that is not visible in the pupillary plane * IOL design not suitable for suturing using capsular bag * patients who are not able to cooperate under measurements * patients with Marfan syndrome and ectopia lentis * exclusion criterion for the control group: other eye surgery.

What they're measuring

IOL position

Timeframe: through study completion, an average of 1,5 years

Capsular thickness

Timeframe: preoperatively or as soon as possible postoperatively

Astigmatism

Timeframe: through study completion, an average of 1,5 years

Trial details

NCT IDNCT04150263

SponsorSt. Erik Eye Hospital

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-05-12

View on ClinicalTrials.gov More Dislocated Intraocular Lens trials