Impact of Iridotomy/Iridectomy Size on Postoperative Pupillary Block and Dysphotopsia Following DMEK

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorUniversity of Leipzig

About this trial

Descemet membrane endothelial keratoplasty (DMEK) is the standard surgical treatment for corneal endothelial disorders. A postoperative pupillary block may occur despite routine preoperative laser iridotomy or intraoperative surgical iridectomy. Insufficient size or incomplete patency of the iridotomy/iridectomy (IT) may contribute to this complication, while excessively large openings may be associated with postoperative dysphotopsia. This prospective observational study investigates the association between IT size measured by anterior segment optical coherence tomography (AS-OCT) and the occurrence of postoperative pupillary block and dysphotopsia after DMEK.

Eligibility criteria

Qualifiers

Adults aged ≥ 18 years

Patients undergoing Descemet membrane endothelial keratoplasty (DMEK) at the Department of Ophthalmology, University Hospital Leipzig

Preoperative Nd:YAG laser iridotomy or intraoperative surgical iridectomy performed as part of standard care

Ability to provide written informed consent

Disqualifiers

Inability to provide informed consent or refusal to participate

Pre-existing surgical iridectomy

Missing or incomplete preoperative or postoperative anterior segment OCT data

Active anterior uveitis or panuveitis at the time of surgery

Trial design

Treatments tested in this trial

  • Anterior Segment Optical Coherence Tomography (AS-OCT)
  • Dysphotopsia Questionnaire

Treatment groups

No treatment groups listed

Locations

This trial has no locations

Sponsors and collaborators