Patient Reported Visual Satisfaction Following Same Day or Delayed Bilateral Cataract Surgery (CatquestCBS)
Primary Purpose
Bilateral Cataract, Charles Bonnet Syndrome
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Immediate sequential bilateral cataract surgery (ISBCS)
Delayed sequential bilateral cataract surgery (DSBCS)
Sponsored by
About this trial
This is an interventional health services research trial for Bilateral Cataract
Eligibility Criteria
Inclusion Criteria:
- Patients planned for bilateral cataract surgery with monofocal intraocular lens implantation in the bag.
- Patients who agree to be randomly allocated to either ISBCS or DSBCS
Exclusion Criteria:
- Patients at risk of intra- og postoperative complications or where delayed visual rehabilitation is expected (e.g. glaucoma, anterior chamber depth 2,3 or less, corneal endothelial dystrophy)
- Patients with axial lengths < 21 mm or > 27 mm
- Patients in need of immediate surgery
- Patients only eligible to one group, e.g. those requiring general anesthesia where ISBCS is the preferred approach
- Patients unable to read, understand or fill out the questionnaire
Sites / Locations
- Department of Ophthalmology, Rigshospitalet-Glostrup
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Immediate sequential bilateral cataract surgery (ISBCS)
Delayed sequential bilateral cataract surgery (DSBCS)
Arm Description
Outcomes
Primary Outcome Measures
Change in patient reported visual function outcome following either ISBCS or DSBCS
Change in participant satisfaction in regards to visual function measured using the Catquest 7-SF questionnaire at the preoperative visit as well as 1 week and 3 months after either ISBCS or 2nd eye surgery in DSBCS
Secondary Outcome Measures
Objective change in visual acuity
Measured using autorefractor
Objective change in refraction status
Measured using autorefractor
Intraocular pressure (IOP)
Measured using I-Care Tonometry
Complications
Incidence of intraoperative and postoperative complications
Presence of corneal edema
Determined during clinical examination using slit lamp
Presence of Charles Bonnet Syndrome
Participants will be asked if they have experienced complex, visual hallucinations during the time in which their vision has been affected by cataract. In case of presence of complex visual hallucinations, patients will be further interviewed regarding the characteristics of the hallucinations.
Knowledge of Charles Bonnet Syndrome
Participants will be asked about previous knowledge of hallucinations caused by loss of vision.
Full Information
NCT ID
NCT05069753
First Posted
September 14, 2021
Last Updated
October 20, 2021
Sponsor
Rigshospitalet, Denmark
1. Study Identification
Unique Protocol Identification Number
NCT05069753
Brief Title
Patient Reported Visual Satisfaction Following Same Day or Delayed Bilateral Cataract Surgery
Acronym
CatquestCBS
Official Title
Patient Reported Visual Function Outcome Following Bilateral Cataract Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
October 2021
Overall Recruitment Status
Unknown status
Study Start Date
November 1, 2021 (Anticipated)
Primary Completion Date
August 31, 2022 (Anticipated)
Study Completion Date
August 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Rigshospitalet, Denmark
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
Cataract is currently the leading cause of visual impairment worldwide with age being the most common cause of lenticular opacification. As cataract surgery is the most commonly performed elective surgery worldwide, forecasts of an increasing number of elderly individuals make it clear that efficient and evidence based models for managing cataract in the future need to be implemented to manage the broadening gap between intervention and available resources.
Bilateral cataract is currently treated using same day separate surgical procedures (immediate sequential bilateral cataract surgery (ISBCS) or on separate days (delayed sequential bilateral cataract surgery (DSBCS). Whether one approach is more ideal than the other is an ongoing debate. There is, however, a clear advantage of same day surgery on resource management.
The primary purpose of this clinical study is to measure the patient reported satisfaction regarding vision in a group of 300 participants following either same day or delayed bilateral cataract surgery.
Detailed Description
In this study, patient reported satisfaction in regards to vision is measured using a questionnaire based on the validated Catquest-7SF questionnaire. This is a 7-item self-report scale with both general questions related to difficulties in performing daily activities and satisfaction with vision, as well as questions assessing performance in specific daily activities. Each question has multiple predefined response categories ranging from "very great difficulty" to "no difficulty". One question has response categories ranging from "very dissatisfied" to "very satisfied". All questions have a "can't say"-response category. Each response will be translated to a numerical value used to score the participants.
In addition to the Catquest-7SF, the questionnaire used will also include questions related to satisfaction with the surgical approach (same day or delayed) and experiences with and knowledge of complex visual hallucinations.
The additional questions about complex visual hallucinations are used to measure prevalence and knowledge of Charles Bonnet Syndrome among participants referred to elective cataract surgery.
The study is a prospective, randomized cohort study and will include 300 consecutive patients referred to our department for elective bilateral cataract surgery. Eligible patients who provide consent will be randomly allocated in a group of either same day bilateral surgery or surgery on two days separated by one week. In case of serious surgical complications in the same day group, surgery of the second eye will be postponed and the participant will be placed in a new, separate group.
During a preoperative visit to the department, participants will fill out the questionnaire regarding vision and be subjected to the routine clinical ophthalmic examination which includes biometry and refraction status. One day post-surgery, participants will be contacted by phone regarding their vision. One-week post-surgery, participants will undergo a check-up visit that includes the same examinations as the preoperative visit, except for biometry. Three months post-surgery, participants will once again be contacted by phone or letter and asked to fill out the questionnaire again.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bilateral Cataract, Charles Bonnet Syndrome
7. Study Design
Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomly allocated to one of two groups using a digital coin toss. Thus they will either undergo same day-surgery of both eyes or have the two surgical procedures separated by one week.
Masking
None (Open Label)
Masking Description
No masking: The patients will be informed of the type of procedure they will undergo.
Allocation
Randomized
Enrollment
300 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Immediate sequential bilateral cataract surgery (ISBCS)
Arm Type
Active Comparator
Arm Title
Delayed sequential bilateral cataract surgery (DSBCS)
Arm Type
Active Comparator
Intervention Type
Procedure
Intervention Name(s)
Immediate sequential bilateral cataract surgery (ISBCS)
Intervention Description
Surgery on both eyes will be performed on the same day as separate procedures: Once surgery on the first eye is completed, a new sterile procedure on the second eye will commence.
Intervention Type
Procedure
Intervention Name(s)
Delayed sequential bilateral cataract surgery (DSBCS)
Intervention Description
The group will undergo bilateral cataract surgery on two separate days with a time period of one week between the two procedures.
Primary Outcome Measure Information:
Title
Change in patient reported visual function outcome following either ISBCS or DSBCS
Description
Change in participant satisfaction in regards to visual function measured using the Catquest 7-SF questionnaire at the preoperative visit as well as 1 week and 3 months after either ISBCS or 2nd eye surgery in DSBCS
Time Frame
Baseline at the preoperative visit, 1 week post-surgery, and 3 months post-surgery
Secondary Outcome Measure Information:
Title
Objective change in visual acuity
Description
Measured using autorefractor
Time Frame
At the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCS
Title
Objective change in refraction status
Description
Measured using autorefractor
Time Frame
At the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCS
Title
Intraocular pressure (IOP)
Description
Measured using I-Care Tonometry
Time Frame
At the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCS
Title
Complications
Description
Incidence of intraoperative and postoperative complications
Time Frame
Intraoperatively, one day after surgery and up to one week after ISBCS or 2nd eye surgery in DSBCS
Title
Presence of corneal edema
Description
Determined during clinical examination using slit lamp
Time Frame
One week after ISBCS or 2nd eye surgery in DSBCS
Title
Presence of Charles Bonnet Syndrome
Description
Participants will be asked if they have experienced complex, visual hallucinations during the time in which their vision has been affected by cataract. In case of presence of complex visual hallucinations, patients will be further interviewed regarding the characteristics of the hallucinations.
Time Frame
At the preoperative visit
Title
Knowledge of Charles Bonnet Syndrome
Description
Participants will be asked about previous knowledge of hallucinations caused by loss of vision.
Time Frame
At the preoperative visit
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients planned for bilateral cataract surgery with monofocal intraocular lens implantation in the bag.
Patients who agree to be randomly allocated to either ISBCS or DSBCS
Exclusion Criteria:
Patients at risk of intra- og postoperative complications or where delayed visual rehabilitation is expected (e.g. glaucoma, anterior chamber depth 2,3 or less, corneal endothelial dystrophy)
Patients with axial lengths < 21 mm or > 27 mm
Patients in need of immediate surgery
Patients only eligible to one group, e.g. those requiring general anesthesia where ISBCS is the preferred approach
Patients unable to read, understand or fill out the questionnaire
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Amardeep Singh, MD, PhD
Phone
+45 20 93 09 49
Email
a.singh.opth@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amardeep Singh, MD, PhD
Organizational Affiliation
Dpt. of Ophthalmology, Rigshospitalet-Glostrup; University of Copenhagen
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Mads Assenholt Nielsen
Organizational Affiliation
Dpt. of Ophthalmology, Rigshospitalet-Glostrup; University of Copenhagen
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Ophthalmology, Rigshospitalet-Glostrup
City
Glostrup
State/Province
Capital Region
ZIP/Postal Code
2600
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
No
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Patient Reported Visual Satisfaction Following Same Day or Delayed Bilateral Cataract Surgery
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