Skip to main content
OpenTrials
Completed

NCT Number: NCT02161263

Quality of Vision and Quality of Life With LASIK

The investigators are administering a validated questionnaire looking at patient reported quality of life and quality of vision after LASIK surgery

Completed

Looking for future studies?

Notify Me

Key information

Age range

21 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Stanford Eye Laser Center

Palo Alto, California, 94303, United States

About this study

The purpose of the study is to evaluate the prevalence of any functional limitations and their associated factors at one, three, six, and twelve months after LASIK surgery and finally the level of patient satisfaction, including the prevalence of any dissatisfaction and its associated factors at one, three, six and twelve months following LASIK surgery using two questionnaires.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Are aged 21 years or older.
  • Have the ability to give informed consent.
  • Speak and read English fluently.
  • Have not previously had any form of refractive surgery, including prior LASIK or cataract surgery.
  • May benefit from increased spectacle independence.
  • Have been determined to be a good candidate for the LASIK procedure based on the investigator's assessment of medical and ophthalmic health, general cognitive function, and physical and social limitations.
  • Have a treatment target of bilateral emmetropia.
  • Express willingness and potential ability to return for all follow-up examinations through the 12-month follow-up exam under the care of the treating investigator.
  • Are not enrolled in any other research study.

Exclusion criteria

  • Subjects under the age of 21.
  • Patients with excessively thin corneas.
  • Patients with topographic evidence of keratoconus.
  • Patients with ectactic eye disorders.
  • Patients with autoimmune diseases.
  • Patients who are pregnant or nursing.

Treatment and study plan

Patient Quality of Life andVision after LASIK Surgery

Other

Patient questionnaire

Primary outcomes

  1. Quality of Vision and Quality of Life Questionnaires after LASIK Surgery

    Time frame: 12 months

    Patients will complete questionnaires preoperatively and postoperatively at month twelve.

Sponsors and collaborators

Lead sponsor

Edward E. Manche

Other

Registry information

Official study title

Patient Quality of Vision and Quality of Life With LASIK Surgery

Important dates

Study start
2014
Primary completion
2023
Study completion
2023
First posted
Jun 11, 2014
Registry last updated
Mar 19, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.