G56.0
Conditions
Interventions
Group 1: Patients with neurologically confirmed carpal tunnel syndrome undergoing surgical treatment are assessed preoperatively and again three months postoperatively using the following instruments:
Sponsors
BG Klinik Tübingen, Klinik für Hand-, Plastische, Rekonstruktive und Verbrennungschirurgie
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Capacity to consent
Exclusion criteria
Exclusion criteria: vulnerable groups, patients undergoing revision surgery, patients with relevant comorbid conditions of the hand
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The aim of this study is to identify psychosocial and clinical factors that influence postoperative outcomes following surgical treatment of carpal tunnel syndrome. Data are collected at two time points: preoperatively and three months postoperatively. To assess patient-reported outcomes, the following instruments are used: Michigan Hand Questionnaire, EuroQoL-5D-5L, Patient Health Questionnaire-4, Pain Catastrophizing Scale and Brief Illness Perception Questionnaire. In addition, standardized clinical parameters and postoperative patient satisfaction are recorded. | — |
Countries
Germany
Contacts
Public ContactJohannes Heinzel
BG Klinik Tübingen, Klinik für Hand-, Plastische, Rekonstruktive und Verbrennungschirurgie
Outcome results
None listed