Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial

Cataract Clinical Trial

— CORE-RCT  

Official title:

Cataract Online Refraction Evaluation: A Multi Center Randomized Controlled Trial

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT04809402
• Other study ID #: NL74625.041.20
• Status: Active, not recruiting
• Phase: N/A
• Start date: April 19, 2021
• Est. completion date: July 22, 2023

Study information

• Verified date: May 2023
• Source: UMC Utrecht
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background of the study:

Cataract is widely prevalent in especially elderly and cataract extraction surgery has thus become one of the most performedsurgeries worldwide. In recent decades the safety of cataract surgery has greatly improved and it is considered one of the safestsurgeries to be performed. Postoperative management consists of routine examinations within one week, to ascertain no adverseevents have occurred immediately after surgery, and between 4-6 weeks, to determine the refractive error. The incidence of seriousadverse events following cataract surgery is estimated to be 1%. As a result, the majority of patient visits after cataract surgery willbe uneventful. Nonetheless valuable time and hospital resources are consumed. Remote monitoring could replace clinicalexaminations in selected patient groups. However, this practice of digital remote monitoring which the patient can use independentlyhas not been clinically validated yet.

Objective of the study:

To determine non-inferiority of the corrected distance visual acuity (CDVA) with the prescription obtained through the web-basedmeasurement of refractive error, compared to usual care, in patients who underwent routine cataract surgery.

Study design:

Observational randomized trial without interventions

Study population:

Patients eligible for cataract surgery, without visual acuity influencing comorbidities or predisposing complicating factors.

Primary study parameters/outcome of the study:

costeffectiveness

Secundary study parameters/outcome of the study (if applicable):

Corrected distance visual acuity at the final post-operative visit, uncorrected distance visual acuity, refractive error(sphere/cylinder/axes), patient reported outcome measurements, adverse events.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 94
• Est. completion date: July 22, 2023
• Est. primary completion date: May 10, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Planned for bilateral phacoemulsification cataract extraction and intra-ocular lens implantation (either sequentialor in one procedure)

• = 18 years of age

• No other current ophthalmic conditions or history that negatively influence post-operative visual acuity

• Be able to fill out the health questionnaires (in Dutch, German or English) and perform the web-based refractiveassessment (possibly with assistance of family member or other close relative).

• Specific digital requirements include access to a computer and a smartphone and knowledge how to log in to anonline patient portal.

Exclusion Criteria:

• Cataract extraction surgery combined with other procedures, including: keratoplasty, vitrectomy, glaucoma filter implants

• Ocular comorbidities that negatively influence post-operative visual acuity

• No access to the digital requirements to take the online health questionnaire and/or perform the online refraction.

• Insufficient command of the Dutch, German or English language to understand the questionnaires andinstructions of the web-based refractive assessment or no family member / close relative to assist with this

• Inability of performing the web-based eye exam prior to cataract surgery.

Related Conditions & MeSH terms

• Cataract

Intervention

Other:
• remote monitoring after cataract surgery
remote monitoring after cataract surgery

Locations

Country	Name	City	State
Austria	Vienna Institute for Research in Ocular Surgery, Austria	Vienna
Germany	Augenklink Sulzbach	Sulzbach
Netherlands	Amphia Ziekenhuis	Breda	Noord-Brabant
Netherlands	Oogcentrum Noordholland	Heerhugowaard	Noord-Holland
Netherlands	Maastricht UMC+	Maastricht
Netherlands	Janneau Claessens	Utrecht

Sponsors (2)

Lead Sponsor	Collaborator
UMC Utrecht	Health Holland

Countries where clinical trial is conducted

Austria,  Germany,  Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cost-effectiveness	The main outcome measure will be Incremental cost-effectiveness ratio (ICER), defined as euros per QALY, and compared between the two groups.	pre-operative until 3 months after surgery
Secondary	Corrected distance visual acuity at the final post-operative visit (achieved with web-based vs manifest refraction)	The corrected distance visual acuity achieved with the web-based refraction will be compared to the corrected distance visual acuity that is achieved with the subjective refraction.	4-6 weeks after surgery
Secondary	Uncorrected distance visual acuity (web-based vs reference chart)	The uncorrected distance visual acuity that is assessed in the web-based assessment will be compared to the uncorrected distance visual acuity that is assessed using the reference chart.	pre-operative, 4-6 weeks after surgery
Secondary	Refractive error in sphere/cylinder/axes (web-based vs reference chart)	The refractive error (in sphere/cylinder/axes) will be asssessed by the web-based assessment and compared to the subjective refractive error assessment.	4-6 weeks after surgery
Secondary	Patient reported outcomes	The PROMs questionnaire (CatQuest-9SF) assesses the patient's own reported visual disability from cataract and the improvement after surgery. High scores represent better visual acuity. The results of the PROMs questionnaire will be compared between the groups to assess differences and determine if a web-based follow-up strategy influences these subjective measures. PROMs will be offered in Dutch, German or English accordingly and assessed at baseline and at 3 months follow-up.	pre-operative vs 3 months after surgery
Secondary	Adverse events / additional consultations	All unplanned additional consultations (telephone or hospital) will be recorded. We will count these and compare the frequencies between the two groups.	pre-operative until 3 months after surgery
Secondary	Total costs	Total costs (in euros) will be determined for both groups. We will count costs for hospital resources and staff, as well as costs for the patient (such as travel and parking costs).	pre-operative until 3 months after surgery
Secondary	QALY's	To determine the QALY, patients of both groups will be requested to fill out questionnaires to assess quality of life (EQ-5D). A unique health state is defined by combining one level from each of the five dimensions. Higher levels indicate more problems.	pre-operative and 3 months after surgery