Qualitative Validation of Patient-Reported Outcomes (PRO) Instrument

NCT03536715 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2018-05-25

No results posted yet for this study

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

  • Patient-Reported Outcomes (PRO)

Sponsors & Collaborators

  • AcuFocus, Inc.

    lead INDUSTRY

Eligibility

Min Age
45 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-06-01
Primary Completion
2017-06-22
Completion
2017-06-22

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03536715 on ClinicalTrials.gov