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Comfort Operative Ocular Light Study (COOL)

Primary Purpose

Cataract

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Ngenuity digital 3D microscope
Conventional microscope
Sponsored by
Fondation Ophtalmologique Adolphe de Rothschild
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cataract focused on measuring Ngenuity 3D digital operating system

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Indication for a first surgery (= first eye to be operated) of cataract alone under topical anesthesia (pure or associated with intravenous sedation)
  • Express consent to participate in the study

Exclusion Criteria:

  • Patient benefiting from a legal protection measure
  • Patient with comprehension problems or who does not understand French well
  • Pregnant or breastfeeding woman
  • Indication for another surgery on the operated side (e.g. vitrectomy combined with cataract surgery)

Sites / Locations

  • Clinique Honoré Cave
  • Hôpital Fondation A. de Rothschuld

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ngenuity digital 3D microscope

Conventional microscope

Arm Description

Outcomes

Primary Outcome Measures

Glare of patients related to the light of the microscope of the patients
Patient response to the question "Were you dazzled by light during surgery?" rated on a numerical scale from 0 (Not at all) to 10 (Yes, very much)

Secondary Outcome Measures

Full Information

First Posted
October 7, 2021
Last Updated
June 30, 2022
Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Collaborators
Alcon Research
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1. Study Identification

Unique Protocol Identification Number
NCT05085314
Brief Title
Comfort Operative Ocular Light Study
Acronym
COOL
Official Title
Prospective Multicenter Randomized Controlled 1:1 Study Evaluating the Efficacy of a 3D Digital Operating Microscope Compared to Conventional Microscopes Microscopes on the Comfort and Subjective Visual Sensations of the Patients Related to the Microscope Light During Initial Cataract Surgery Under Topical Anesthesia Topical Anesthesia
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
November 18, 2021 (Actual)
Primary Completion Date
June 1, 2022 (Actual)
Study Completion Date
June 1, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fondation Ophtalmologique Adolphe de Rothschild
Collaborators
Alcon Research

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Digital 3D microscopes require less light and may be more comfortable for patients requiring cataract surgery under topical anesthesia compared to conventional microscopes. To date, no studies have evaluated the comfort and subjective visual sensations related to the light of the 3D digital microscope in cataract surgery patients. The purpose of this study is to evaluate the effectiveness of the Ngenuity 3D digital operating system (Alcon, Fort Worth, TX) compared to conventional microscopes on the comfort and subjective visual sensations related to of patients undergoing initial cataract surgery under topical anesthesia (pure or combined with intravenous sedation).
Detailed Description
Patients will be recruited during the preoperative consultation where the indication for cataract surgery. The allocation of the management arm (3D digital microscope or conventional microscope) will be randomized in a stratified way on the center. Prior to his or her operative session, the surgeon will set up the microscope with his or her usual parameters. The light intensity will be measured at the beginning of the operating session with a calibrated light meter. The type of anesthesia (pure topical or associated with intravenous sedation), the duration of the operation, intraoperative complications (frequency and type), and the possible use of an anesthesiologist to inject additional intravenous anesthetic will be collected. Before the patient is discharged from the ambulatory surgical unit, the clinical study technician will ask the patient the 4 questions of the standardized questionnaire assessing comfort and subjective visual sensations related to the microscope light.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cataract
Keywords
Ngenuity 3D digital operating system

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
134 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ngenuity digital 3D microscope
Arm Type
Experimental
Arm Title
Conventional microscope
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Ngenuity digital 3D microscope
Intervention Description
Cataract surgery under topical anesthesia with the Ngenuity digital 3D microscope, Alcon, Fort Worth, TX
Intervention Type
Procedure
Intervention Name(s)
Conventional microscope
Intervention Description
Cataract surgery under topical anesthesia with a conventional microscope
Primary Outcome Measure Information:
Title
Glare of patients related to the light of the microscope of the patients
Description
Patient response to the question "Were you dazzled by light during surgery?" rated on a numerical scale from 0 (Not at all) to 10 (Yes, very much)
Time Frame
two hours maximum after surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Indication for a first surgery (= first eye to be operated) of cataract alone under topical anesthesia (pure or associated with intravenous sedation) Express consent to participate in the study Exclusion Criteria: Patient benefiting from a legal protection measure Patient with comprehension problems or who does not understand French well Pregnant or breastfeeding woman Indication for another surgery on the operated side (e.g. vitrectomy combined with cataract surgery)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ramin TADAYONI
Organizational Affiliation
Hôpital Fondation A. de Rothschild
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Vincent GUALINO
Organizational Affiliation
Clinique Honoré Cave, Montauban
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Aude COUTURIER
Organizational Affiliation
Hôpital Lariboisière
Official's Role
Study Chair
Facility Information:
Facility Name
Clinique Honoré Cave
City
Montauban
ZIP/Postal Code
82000
Country
France
Facility Name
Hôpital Fondation A. de Rothschuld
City
Paris
ZIP/Postal Code
75019
Country
France

12. IPD Sharing Statement

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Comfort Operative Ocular Light Study

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