ClinicalTrials.Veeva

Menu

Eyelid Closure in Keratometry

V

Vienna Institute for Research in Ocular Surgery

Status

Enrolling

Conditions

Dry Eye
Ocular Surface Disease

Treatments

Behavioral: Eyelid closure for 3 minutes

Study type

Interventional

Funder types

Other

Identifiers

NCT07297849
EK 24-111-0824

Details and patient eligibility

About

Cataract surgery is one of the most common performed surgeries in the world. While in the early beginnings of cataract surgery, visual rehabilitation was the main goal of the procedure, refractive outcome and subsequent relative spectacles independency is gaining increasing importance in patients' demands. Due to the improvements in measurement techniques and prediction formulas, the prediction of postoperative refraction is possible with high accuracy. However, there are still some sources of error that lead to deviations of predicted postoperative refraction. For instance, it was shown that tear film osmolarity, an established biomarker for dry eye disease (DED), plays an important role in preoperative precision of keratometry measurements. Keratometry, the measurement of corneal curvature, is an important part of preoperative biometry. Errors in preoperative keratometry measurements lead to nearly one-to-one deviations from the predicted refraction. Therefore, proper keratometry measurements are a key element in intraocular lens (IOL) power calculations. To counteract the issue of DED in preoperative biometry, the principle of using lubricating eye drops before ocular biometry has been investigated and it was shown that the use of ocular lubricants may lead to increased variability of keratometry measurements. From our clinical observations, another possible mechanism to improve keratometry is eyelid closure for some minutes. In contrast to the long-term use of ocular lubricants to stabilize the tear film, eyelid closure is an easy and fast intervention to possibly improve the precision of keratometry measurements. Additionally, a clinical trial investigating the usage of lubricating eye drops for two weeks found no improvement of variability of keratometry in DED patients.

Therefore, this study aims to investigate the effect of eyelid closure on the quality index of keratometric measurements in patients with a warning for the quality of keratometric measurements. For this purpose, a single study day including 4 repeated measurements (2 without and 2 with lid closure for 3 minutes) using an ocular biometer (IOLMaster700) will be performed.

Enrollment

29 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 or older
  • Written informed consent
  • Keratometry quality index "warning"

Exclusion criteria

  • Severe corneal conditions that may compromise corneal integrity (such as corneal scarring, etc.)
  • Pregnancy (pregnancy test will be taken in women of reproductive age), nursing women
  • Ocular surgery in the study eye in the three months preceding the study
  • Inability of visual fixation (e.g. in patients with nystagmus)
  • Inability of eyelid closure (e.g. in patients with facial nerve paralysis)

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Sequential Assignment

Masking

None (Open label)

29 participants in 1 patient group

Patients with a keratometrical warning index
Experimental group
Description:
The following measurements will be performed in the mentioned order during the visit 1 only in the randomized study eye: 1. First and second biometry using IOLMaster® 700 (2x, 3 minutes pause between the measurements, eyes open, normal blinking) 2. Eyelid closure for 3 minutes 3. Third biometry using IOLMaster® 700 (1x) right after opening of the eyelid 4. Eyelid closure for 3 minutes 5. Fourth biometry using IOLMaster® 700 (1x) right after opening of the eyelid
Treatment:
Behavioral: Eyelid closure for 3 minutes

Trial contacts and locations

1

Loading...

Central trial contact

Andreas Schlatter, MD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems