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OSUWMC EEI Sequential Cataract Patient Experience Project

OSUWMC EEI Sequential Cataract Patient Experience Project

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03002688
Enrollment
286
Registered
2016-12-26
Start date
2017-01-31
Completion date
2018-03-31
Last updated
2018-04-11

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

Conditions

Cataract Surgery Experience

Brief summary

The purpose is to gauge the patients' level of comfort and anxiety for sequential cataract surgeries to assess if the second experience of cataract surgery differs from the initial experience.

Detailed description

Each patient is scheduled to undergo two sequential cataract extractions under topical anesthesia with local anesthetic eye drops and minimal sedation- one on each eye. The surgeon, basic surgical procedure, anesthetic technique, and approximate length of procedure are reasonably similar and the patients act as their own control. Subjects in the study will answer very brief questions regarding anxiety and comfort about their surgery before and after each procedure, and on the day after their second surgery.

Interventions

OTHERSurvey

Verbal survey will be given before and after the cataract surgery, and on the day following the second cataract surgery.

Sponsors

Ohio State University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

1. Patients undergoing sequential cataract surgeries within a 6 week time period performed by the ophthalmologist, Amit Tandon, MD. 2. Aged 18 years and older.

Exclusion criteria

1. Cognitive impairment causing inability to participate in survey 2. Language barrier causing an inability to participate in survey 3. Healthcare POA or guardian leading to an inability to consent to survey 4. Physician autonomy; patients that are inappropriate for the study as deemed by investigator

Design outcomes

Primary

MeasureTime frameDescription
PainFirst and second cataract extraction surgery occuring within 6 weeksPain will be evaluated using verbal survey after each cataract surgery, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in pain between surgeries on the day after the second cataract surgery.
AnxietyFirst and second cataract extraction surgery occuring within 6 weeksAnxiety will be evaluated using verbal survey before each cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in anxiety between surgeries on the day after the second cataract surgery.
AwarenessFirst and second cataract extraction surgery occuring within 6 weeksAwareness will be evaluated using verbal survey after each cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in awareness between surgeries on the day after the second cataract surgery.
Comfort LevelFirst and second cataract extraction surgery occuring within 6 weeksComfort level will be evaluated using verbal survey after cataract surgeries, scheduled to occur within 6 weeks time; subject will be asked if there was any difference in comfort level between surgeries on the day after the second cataract surgery.

Countries

United States

Outcome results

None listed

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