A Study to Validate the Patient-Specific Functional Survey in Patients with Carpal Tunnel Syndrome


  • Study type

  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 19-002076
    Sponsor Protocol Number: 19-002076

About this study

The purpose of this study is to determine if the Patient-Specific Functional Survey (PSFS) is a valid and reliable measure to evaluate functional difficulties with 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. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria:

  • All new patients (>18 years) visiting the Orthopaedic Hand Service with the diagnosis of carpal tunnel syndrome.
  • Return patients (>18 years) with carpal tunnel syndrome previously treated with splinting who decide to proceed with surgery.
  • English fluency and literacy.
  • Able to take informed consent.

Exclusion Criteria: 

  • Age less than 18 years old.
  • Additional ipsilateral hand issue in addition to carpal tunnel syndrome.

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

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.



More information


Publications are currently not available

Study Results Summary

Not yet available

Supplemental Study Information

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