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Influencing Factors of the Corneal Endothelial Cell Loss (PREDICS)

C

Centre Hospitalier Régional Metz-Thionville

Status

Completed

Conditions

Cataract

Treatments

Procedure: Phacoemulsification

Study type

Interventional

Funder types

Other

Identifiers

NCT05265832
2021-04-CHRMT

Details and patient eligibility

About

This is a multi-center cohort study with prognostic aims to identify factors associated with endothelial cell loss during cataract surgery.

Patients will have their endothelial density measured by specular microscopy preoperatively, at 1 month and at 3 months after surgery. The rest of their management will be in line with standard practice.

Full description

Cataract surgery is the most commonly performed surgical procedure worldwide. Postoperative visual function depends on implant into the crystalline lens, retinal lesion, corneal damage or glaucomatous damage. Moreover, preoperative corneal endothelial damage should be as low as possible to provide corneal transparency. Indeed, the endothelium plays important role in maintaining corneal transparency.

The loss rate of endothelial cell after cataract surgery ranges in the scientific literature from 8 to 15 %. Severe endothelial cell loss contributes to corneal edema. This edema resulting in a loss of visual acuity and may require corneal transplantation as a last resort.

Various studies describe some factors that affecting endothelial cell loss such as the cataract density, pupil abnormalities (small diameter), Advanced age or short axial length.

However, few studies have been demonstrated the link between endothelial cell loss and the volume of fluid used during the intervention or the use of intracamerular substances. This study wants to establish a correlation between endothelial cell loss and predictive factors. Thus, knowledge of these factors would have ensured a better control of endothelial dysfunction.

Enrollment

154 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients undergoing cataract surgery
  • Visual acuity monoyer scale <8/10e (> +0.2 logMar)
  • Nuclear, cortical and posterior subcapsular cataract with normal density to severe in the LOCSIII classification
  • Covered by the social security scheme
  • Have given their oral agreement

Exclusion criteria

  • Corneal disease: keratitis, dystrophy or corneal degeneration
  • Any disease of the anterior segment
  • Low preoperative endothelial cell density <1000 c/mm²
  • Pregnancy, lactation
  • Risk factors for surgical per-operative complication
  • Uncontrolled ocular pressure
  • Combined surgery (cataract with corneal graft, cataract with glaucoma surgery, cataract with vitrectomy, ....)
  • Under legal protection

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

154 participants in 1 patient group

Cataract surgery
Experimental group
Description:
Phacoemulsification cataract surgery
Treatment:
Procedure: Phacoemulsification

Trial contacts and locations

2

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Central trial contact

Sandra MARCHIONNI; Jean Marc Perone, MD

Data sourced from clinicaltrials.gov

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