Study to Analyze Patient Preferences in Outcome Measurements of Patients with Carpal Tunnel Syndrome

Overview

About this study

The purpose of this study is to elicit patient preference for patient-reported outcome measures in carpal tunnel syndrome.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Please contact the study team to discuss whether or not you are eligible to participate in a study.

Inclusion Criteria:

  • All new and follow-up patients visiting the orthopaedic hand service with suspected (later confirmed) or diagnosed carpal tunnel syndrome.
  • Diagnosis with either CTS-6 score of 12.5 or greater, or positive nerve velocity.
  • Unilateral or bilateral.
  • Adults (age 18 and over).
  • English fluency and literacy.
  • Able to take informed consent.

Exclusion Criteria: 

  • Language barriers to completing questionnaire.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Sanjeev Kakar, M.D.

Contact us for the latest status

Contact information:

Sanjeev Kakar M.D.

(507) 284-4828

Kakar.Sanjeev@mayo.edu

More information

Publications

Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

Not yet available

.
CLS-20441826

Mayo Clinic Footer