Phantom limb pain
Conditions
Interventions
Group 1: pre- and acute postoperative evaluation (POD 0-5) of pain levels during amputation
Sponsors
UK Essen
Eligibility
Sex/Gender
All
Age
12 Years to No maximum
Inclusion criteria
Inclusion criteria: Amputation surgery In domo =3 days Signed declaration of consent based on the Declaration of Helsinki, if < 18 years by legal guardian
Exclusion criteria
Exclusion criteria: Diagnosis of dementia, cognitive impairment Lack of consent Insufficient knowledge of German
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Reduction of Numeric Rating scale (NRS) on post-OP day (POD) 0-5 | — |
Secondary
| Measure | Time frame |
|---|---|
| - Longitudinal survey of the frequency of phantom pain - Evaluation of predictors for PLP and/or RLP Pain level: preoperative, postoperative and long-term Cause of amputation (tumour / traumatic / vascular) Extent of amputation (e.g. major amputation as a risk factor) Perioperative anaesthesiological regime, e.g. general anaesthesia, regional anaesthesia (procedure) +/- analgosedation Therapy regime after discharge Use of orthoses Socio-demographic data, e.g. age, gender, educational level, social status, handedness Psychological comorbidities: Depression, anxiety disorder - Evaluation of the side effects of ketamine during application | — |
Countries
Germany
Contacts
Public ContactBeatrice Oehler
UK Essen
Outcome results
None listed