Trials / Completed
CompletedNCT03536715
Qualitative Validation of Patient-Reported Outcomes (PRO) Instrument
Qualitative Patient Interviews to Develop a Patient-Reported Outcomes (PRO) Instrument to Assess Visual Symptoms in KAMRA® Inlay Patients
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 22 (actual)
- Sponsor
- AcuFocus, Inc. · Industry
- Sex
- All
- Age
- 45 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to conduct concept elicitation and cognitive debriefing interviews with patients who have been implanted with the KAMRA inlay in order to assess the content validity of a PRO instrument
Conditions
Timeline
- Start date
- 2016-06-01
- Primary completion
- 2017-06-22
- Completion
- 2017-06-22
- First posted
- 2018-05-25
- Last updated
- 2018-05-25
Source: ClinicalTrials.gov record NCT03536715. Inclusion in this directory is not an endorsement.