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Patient Reported Visual Satisfaction Following Same Day or Delayed Bilateral Cataract Surgery

Patient Reported Visual Function Outcome Following Bilateral Cataract Surgery

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05069753
Acronym
CatquestCBS
Enrollment
300
Registered
2021-10-06
Start date
2021-11-01
Completion date
2022-08-31
Last updated
2021-10-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bilateral Cataract, Charles Bonnet Syndrome

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.

Interventions

PROCEDUREImmediate sequential bilateral cataract surgery (ISBCS)

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.

PROCEDUREDelayed sequential bilateral cataract surgery (DSBCS)

The group will undergo bilateral cataract surgery on two separate days with a time period of one week between the two procedures.

Sponsors

Rigshospitalet, Denmark
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Masking description

No masking: The patients will be informed of the type of procedure they will undergo.

Intervention 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.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change in patient reported visual function outcome following either ISBCS or DSBCSBaseline at the preoperative visit, 1 week post-surgery, and 3 months post-surgeryChange 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

MeasureTime frameDescription
Objective change in refraction statusAt the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCSMeasured using autorefractor
Intraocular pressure (IOP)At the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCSMeasured using I-Care Tonometry
ComplicationsIntraoperatively, one day after surgery and up to one week after ISBCS or 2nd eye surgery in DSBCSIncidence of intraoperative and postoperative complications
Objective change in visual acuityAt the preoperative visit and 1 week after ISBCS or 2nd eye surgery in DSBCSMeasured using autorefractor
Presence of Charles Bonnet SyndromeAt the preoperative visitParticipants 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 SyndromeAt the preoperative visitParticipants will be asked about previous knowledge of hallucinations caused by loss of vision.
Presence of corneal edemaOne week after ISBCS or 2nd eye surgery in DSBCSDetermined during clinical examination using slit lamp

Countries

Denmark

Contacts

Primary ContactAmardeep Singh, MD, PhD
a.singh.opth@gmail.com+45 20 93 09 49

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026