MYFLACS: Evaluation of a Protocol of Pupil Dilation Before Laser-assisted Cataract Surgery

Sponsor
CHU de Reims (Other)
Overall Status
Unknown status
CT.gov ID
NCT03375996
Collaborator
(none)
60
1
23
2.6

Study Details

Study Description

Brief Summary

Laser-assisted cataract surgery is an innovative and growing procedure to improve the safety and results of modern cataract surgery. However, this technique faces to some obstacles: economics in the one hand due to the cost and time spent for the laser procedure before the conventional surgery, and technical in the other hand, especially due to some loss of pupil dilation during the surgery, which is highly important to ensure a perfect procedure. The present study aims at assessing a pharmacological protocol to maintain an accurate pupil dilation all along the surgery in order to improve the whole procedure.

Condition or Disease Intervention/Treatment Phase
  • Drug: cyclopentolate 0.5% eye drops

Detailed Description

Femtosecond laser-assisted cataract surgery (FLACS) is a major surgical development that would allow systematization of surgery and even improved safety of the procedure. The development of this new surgical technique must now face certain obstacles, in particular (i) financial considering the extra cost generated by the use of the laser and (ii) technique due to the need to re-learn certain gestures and certain variations related to the laser procedure and more specifically the instability of the pupillary mydriasis (dilatation) during the actual surgery. The use of a systematic preoperative pharmacological mydriasis protocol should allow maximum intraoperative mydriasis to be maintained, allowing satisfactory surgery throughout the procedure. Several drugs or medical devices are now indicated in cataract surgery, but their effectiveness has not been specifically evaluated for the laser technique. This study could thus make it possible to validate or not a protocol of mydriasis that could make consensus in the future for the practice of FLACS.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Evaluation of a Preoperative Pharmacological Protocol for Mydriasis in Femtosecond Laser-assisted Cataract Surgery
Actual Study Start Date :
Jun 1, 2018
Anticipated Primary Completion Date :
Mar 1, 2020
Anticipated Study Completion Date :
May 1, 2020

Arms and Interventions

Arm Intervention/Treatment
FLACS group

Patient presenting cataract and scheduled for laser-assisted cataract surgery

Drug: cyclopentolate 0.5% eye drops
cyclopentolate 0.5% eye drops and measurement of the pupillary mydriasis (dilatation)

Outcome Measures

Primary Outcome Measures

  1. Pupil diameter > 6 mm all along the surgical procedure [Day 0]

    a posteriori pupil measurement using the peroperative movie recorded via the operative microscope during each surgery.

Secondary Outcome Measures

  1. Pupil diameter variation at each time of the surgery [Day 0]

  2. Surgeon satisfaction [Day 0]

    questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No

inclusion criteria :

  • Patient with unilateral or bilateral cataract requiring a cataract surgery

  • Patient scheduled for laser-assisted cataract surgery

exclusion criteria :

  • Limitation due to laser procedure (little orbits, corneal scares, lack of pharmacological mydriasis at the inclusion visit)

  • Subject with general medication influencing iris state and/or pupil dilation (alpha-agonist, psychotropic drugs)

  • Subject unable to give informed consent

  • minors

Contacts and Locations

Locations

Site City State Country Postal Code
1 Chu Reims Reims France 51092

Sponsors and Collaborators

  • CHU de Reims

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
CHU de Reims
ClinicalTrials.gov Identifier:
NCT03375996
Other Study ID Numbers:
  • PO17111
First Posted:
Dec 18, 2017
Last Update Posted:
Dec 16, 2019
Last Verified:
Dec 1, 2019
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 16, 2019