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Retrospective Patient Satisfaction Survey in Subjects With Tecnis Intra Ocular Lenses and Cataracts Surgery

Retrospective Patient Satisfaction Survey in Subjects With Tecnis Intra Ocular Lenses Cataracts Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01946581
Enrollment
200
Registered
2013-09-19
Start date
2013-05-31
Completion date
Unknown
Last updated
2013-09-19

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

Conditions

Cataract

Brief summary

Define what factors correlate with higher degrees of patient satisfaction and dissatisfaction among patients who have recently undergone cataract surgery.

Interventions

PROCEDURECataract Surgery

Sponsors

MDbackline, LLC
Lead SponsorOTHER

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients with uncomplicated bilateral cataract surgery with a Tecnis Multifocal or monofocal implant completed at least 60 days before the survey date. * Patient with and without astigmatic keratotomy will be included.

Exclusion criteria

* Patients with visually significant co-morbidities (corneal, retina, optic nerve disease) that could affect their satisfaction with surgery * Patients with surgical complications either during or after surgery (capsule tears, iris trauma, decentered IOL, cystoid macular edema, etc.) * Patients with ≥ grade 1 posterior capsule opacity at their last visit

Design outcomes

Primary

MeasureTime frameDescription
Patient overall satisfaction post Cataract surgery60 plus days Post surgeryPatient will be given a satisfaction survey based on overall satisfaction: * Motivations for choosing their surgeon and for selecting an IOL choice * Fears that they had before surgery * Degree of spectacle independence for activities, including driving (day and night), watching television, computer use, reading print material, using their mobile phone * Degree of overall satisfaction with vision * Degree to which they notice unexpected side effects (dysphotopsias) * Degree to which they felt informed about any side effects they did experience * Activities for which they would like to see better * Willingness to refer friends for the same surgery * Whether they have already referred friends for the same surgery

Countries

United States

Contacts

Primary ContactCarol Hardy
research@harvardeye.com949-900-5248

Outcome results

None listed

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