Cost-effectiveness of ISBCS vs. DSBCS
Primary Purpose
Bilateral Cataract
Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
ISBCS
DSBCS
Sponsored by
About this trial
This is an interventional treatment trial for Bilateral Cataract
Eligibility Criteria
Inclusion Criteria:
- Bilateral cataract
- Indication for bilateral cataract surgery
- Expected uncomplicated surgery
Exclusion Criteria:
- Inability to comply with study procedures or to complete follow-up / Dutch questionnaires.
- Non-routine cataract surgery
- Cognitive or behavioural conditions that might interfere with surgery
- Cataract surgery with premium IOL implantation
- Conditions that increase the risk of endophthalmitis (e.g. current ocular/adnexal/periocular infections, immune-compromised, iodine allergy)
- Factors that increase the risk of refractive surprise (e.g. axial lengths <21mm or >27mm, difference between eyes of >1.5mm, abnormal keratometry readings, previous refractive surgery)
- Conditions that increase the risk of corneal edema
- Factors that increase the risk of complicated surgery (e.g. previous surgery, trauma, anatomical abnormalities)
- Sight-threatening comorbidity, Glaucoma or IOP > 24mmHg, Uveitis, Diabetes with diabetic retinopathy and macular edema
Sites / Locations
- Maastricht University Medical Center (MUMC+)
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
ISBCS
DSBCS
Arm Description
The intervention group will undergo cataract surgery of both eyes on the same day (ISBCS)
The usual care / control group will undergo cataract surgery of both eyes on separate days, with a time period of at least two weeks between surgeries (DSBCS).
Outcomes
Primary Outcome Measures
Refraction: deviation of 1.0 D from target refraction
Proportion of patients in both treatment groups with a postoperative refraction in the second eye that deviates 1.0 diopters (D) from target refraction
Secondary Outcome Measures
Refraction: deviation of 0.5 D from target refraction
Proportion of patients in both treatment groups with a postoperative refraction in the second eye that deviates 0.5 diopters (D) from target refraction
Change in visual acuity
Visual acuity will be measured by ETDRS letter charts
Complications
The incidence of intraoperative and postoperative complications
Patient reported outcome measures (PROMs): NEI VFQ-25
Patient satisfaction and vision-specific quality of life as measured by National Eye Institute Visual Function Questionnaire (NEI VFQ-25).
Patient reported outcome measures (PROMs): Catquest
Patient satisfaction and vision-specific quality of life as measured by Catquest questionnaire.
Patient reported outcome measures (PROMs): HUI3
Health-related quality of life as measured by HUI3 (Health Utility Index Mark 3) questionnaire.
Patient reported outcome measures (PROMs): EQ-5D-5L
Health-related quality of life as measured by EQ-5D-5L questionnaire.
Quality Adjusted Life Years (QALYs)
Calculated based on generic health-related quality of life, using the EQ-5D-5L and HUI-3 questionnaires
Costs per patient
Cost per patient, including valuation of resource use by using the Dutch guidelines for cost-analyses or cost prices provided by the medical center.
Incremental cost-effectiveness ratios (ICERs): QALY
Evaluation of cost-effectiveness by using calculated costs per quality-adjusted life years (QALYs)
Incremental cost-effectiveness ratios (ICERs): Target refraction
Calculated costs per patient with a postoperative refraction within 1.0 D of target refraction
Incremental cost-effectiveness ratios (ICERs): NEI VFQ-25
Calculated costs per clinically improved patient on the NEI VFQ-25 questionnaire
Incremental cost-effectiveness ratios (ICERs): Catquest
Calculated costs per clinically improved patient on the Catquest questionnaire
Incremental cost-effectiveness ratios (ICERs): Visual acuity
Calculated costs per patient with clinical improvement in (un)corrected distance visual acuity
Budget impact
Reported as a difference in costs. Different scenario's will be compared to investigate the impact of various levels of implementation (e.g. 25%, 50%, 75% of eligible patients).
Full Information
NCT ID
NCT03400124
First Posted
December 22, 2017
Last Updated
September 3, 2021
Sponsor
Maastricht University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
1. Study Identification
Unique Protocol Identification Number
NCT03400124
Brief Title
Cost-effectiveness of ISBCS vs. DSBCS
Official Title
Cost-effectiveness of Immediately Versus Delayed Sequential Bilateral Cataract Surgery (ISBCS vs. DSBCS)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
September 1, 2018 (Actual)
Primary Completion Date
October 1, 2020 (Actual)
Study Completion Date
February 1, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center
Collaborators
ZonMw: The Netherlands Organisation for Health Research and Development
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the effectiveness and costs of immediately sequential bilateral cataract surgery (ISBCS) compared to delayed sequential bilateral cataract surgery (DSBCS) in order to determine whether ISBCS is an effective and cost-effective alternative to DSBCS.
Detailed Description
With an estimated number of 180,000 cataract extractions per year in the Netherlands, cataract surgery is one of the most frequently performed types of surgery. The majority of patients suffer from bilateral cataract and while cataract surgery of one eye is effective in restoring functional vision, second-eye surgery leads to further improvement in health-related quality of life.
Currently, most patients undergo cataract surgery in both eyes on separate days as recommended in national guidelines, referred to as delayed sequential bilateral cataract surgery (DSBCS). An alternative procedure involves cataract surgery of both eyes on the same day, but as separate procedures, known as immediately sequential bilateral cataract surgery (ISBCS).
Potential benefits of ISBCS include less time between surgeries, a faster total recovery period and lower costs. Potential risks, however, are complications of cataract surgery in general, most importantly the risk of endophthalmitis and refractive surprise. In ISBCS, both eyes are at risk at the same time, while in DSBCS both eyes are exposed to these risks consecutively.
Since there is no consensus yet about the role of ISBCS in current regular practice, further investigation of functional and surgical outcomes and cost-effectiveness of ISBCS compared to DSBCS is required. Therefore, the purpose of this study is to evaluate the effectiveness and costs of ISBCS compared to DSBCS, in order to determine whether ISBCS is an effective and cost-effective alternative to DSBCS.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bilateral Cataract
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
858 (Actual)
8. Arms, Groups, and Interventions
Arm Title
ISBCS
Arm Type
Active Comparator
Arm Description
The intervention group will undergo cataract surgery of both eyes on the same day (ISBCS)
Arm Title
DSBCS
Arm Type
Active Comparator
Arm Description
The usual care / control group will undergo cataract surgery of both eyes on separate days, with a time period of at least two weeks between surgeries (DSBCS).
Intervention Type
Procedure
Intervention Name(s)
ISBCS
Intervention Description
The intervention group will undergo cataract surgery in both eyes on the same day (ISBCS)
Intervention Type
Procedure
Intervention Name(s)
DSBCS
Intervention Description
The usual care / control group will undergo cataract surgery in both eyes on separate days, with a time period of at least two weeks between surgeries.
Primary Outcome Measure Information:
Title
Refraction: deviation of 1.0 D from target refraction
Description
Proportion of patients in both treatment groups with a postoperative refraction in the second eye that deviates 1.0 diopters (D) from target refraction
Time Frame
Four weeks post-operatively
Secondary Outcome Measure Information:
Title
Refraction: deviation of 0.5 D from target refraction
Description
Proportion of patients in both treatment groups with a postoperative refraction in the second eye that deviates 0.5 diopters (D) from target refraction
Time Frame
Four weeks post-operatively
Title
Change in visual acuity
Description
Visual acuity will be measured by ETDRS letter charts
Time Frame
Baseline, 1 week after first-eye surgery and 4 weeks after second-eye surgery
Title
Complications
Description
The incidence of intraoperative and postoperative complications
Time Frame
Intraoperatively and up to 4 weeks after second-eye surgery
Title
Patient reported outcome measures (PROMs): NEI VFQ-25
Description
Patient satisfaction and vision-specific quality of life as measured by National Eye Institute Visual Function Questionnaire (NEI VFQ-25).
Time Frame
Baseline and 3 months postoperatively
Title
Patient reported outcome measures (PROMs): Catquest
Description
Patient satisfaction and vision-specific quality of life as measured by Catquest questionnaire.
Time Frame
Baseline and 3 months postoperatively
Title
Patient reported outcome measures (PROMs): HUI3
Description
Health-related quality of life as measured by HUI3 (Health Utility Index Mark 3) questionnaire.
Time Frame
Baseline, 1,4 weeks and 3 months postoperatively
Title
Patient reported outcome measures (PROMs): EQ-5D-5L
Description
Health-related quality of life as measured by EQ-5D-5L questionnaire.
Time Frame
Baseline, 1,4 weeks and 3 months postoperatively
Title
Quality Adjusted Life Years (QALYs)
Description
Calculated based on generic health-related quality of life, using the EQ-5D-5L and HUI-3 questionnaires
Time Frame
Baseline until 3 months postoperatively
Title
Costs per patient
Description
Cost per patient, including valuation of resource use by using the Dutch guidelines for cost-analyses or cost prices provided by the medical center.
Time Frame
Baseline until 3 months postoperatively
Title
Incremental cost-effectiveness ratios (ICERs): QALY
Description
Evaluation of cost-effectiveness by using calculated costs per quality-adjusted life years (QALYs)
Time Frame
Baseline until 3 months postoperatively
Title
Incremental cost-effectiveness ratios (ICERs): Target refraction
Description
Calculated costs per patient with a postoperative refraction within 1.0 D of target refraction
Time Frame
Baseline until 3 months postoperatively
Title
Incremental cost-effectiveness ratios (ICERs): NEI VFQ-25
Description
Calculated costs per clinically improved patient on the NEI VFQ-25 questionnaire
Time Frame
Baseline until 3 months postoperatively
Title
Incremental cost-effectiveness ratios (ICERs): Catquest
Description
Calculated costs per clinically improved patient on the Catquest questionnaire
Time Frame
Baseline until 3 months postoperatively
Title
Incremental cost-effectiveness ratios (ICERs): Visual acuity
Description
Calculated costs per patient with clinical improvement in (un)corrected distance visual acuity
Time Frame
Baseline until 3 months postoperatively
Title
Budget impact
Description
Reported as a difference in costs. Different scenario's will be compared to investigate the impact of various levels of implementation (e.g. 25%, 50%, 75% of eligible patients).
Time Frame
Baseline until 3 months postoperatively
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Bilateral cataract
Indication for bilateral cataract surgery
Expected uncomplicated surgery
Exclusion Criteria:
Inability to comply with study procedures or to complete follow-up / Dutch questionnaires.
Non-routine cataract surgery
Cognitive or behavioural conditions that might interfere with surgery
Cataract surgery with premium IOL implantation
Conditions that increase the risk of endophthalmitis (e.g. current ocular/adnexal/periocular infections, immune-compromised, iodine allergy)
Factors that increase the risk of refractive surprise (e.g. axial lengths <21mm or >27mm, difference between eyes of >1.5mm, abnormal keratometry readings, previous refractive surgery)
Conditions that increase the risk of corneal edema
Factors that increase the risk of complicated surgery (e.g. previous surgery, trauma, anatomical abnormalities)
Sight-threatening comorbidity, Glaucoma or IOP > 24mmHg, Uveitis, Diabetes with diabetic retinopathy and macular edema
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rudy Nuijts, PhD
Organizational Affiliation
Department of Ophthalmology, Maastricht University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maastricht University Medical Center (MUMC+)
City
Maastricht
State/Province
Limburg
ZIP/Postal Code
6229 HX
Country
Netherlands
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
32600295
Citation
Spekreijse LS, Simons RWP, Winkens B, van den Biggelaar FJHM, Dirksen CD, Nuijts RMMA. Cost-effectiveness of immediate versus delayed sequential bilateral cataract surgery in the Netherlands (the BICAT-NL study): study design of a prospective multicenter randomised controlled trial. BMC Ophthalmol. 2020 Jun 29;20(1):257. doi: 10.1186/s12886-020-01521-x.
Results Reference
derived
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Cost-effectiveness of ISBCS vs. DSBCS
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