Lacertus syndrome, Pronator Teres syndrome, Carpal tunnel syndrome
Conditions
Interventions
Lacertus surgery, ultrasound, EMG
Sponsors
Erasmus MC, Universitair Medisch Centrum Rotterdam
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Presenting with median neuropathy symptoms and/or clinically suspected lacertus syndrome.
Exclusion criteria
Exclusion criteria: Inability to provide consent, language barriers or patients in police custody
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary study parameters are the descriptive findings from clinical evaluation, ultrasound, and electrodiagnostic testing in patients with suspected lacertus syndrome. In patients undergoing surgery, changes in these findings will be analyzed postoperatively. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints include improvements in: • Motor function (e.g., MRC scale, pinch strength), • Sensory function (e.g., BMRC, Semmes-Weinstein), • Patient-reported outcomes (e.g., VAS pain/function, BCTQ, EQ-5D, satisfaction, and return to work). | — |
Countries
Netherlands
Contacts
Public ContactX Smit
Erasmus MC, Universitair Medisch Centrum Rotterdam
Outcome results
None listed