Dupuytren’s disease Musculoskeletal Diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Adults aged =18 years undergoing PNA for Dupuytren’s disease 2. Disease affecting a single hand with one or more involved rays 3. Able to provide informed consent
Exclusion criteria
Exclusion criteria: 1. Known allergy or hypersensitivity to lignocaine 2. Prior sensory deficit or paraesthesia in the affected hand 3. Cognitive impairment affecting reliable pain assessment 4. Inability to provide informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Injection pain measured using a 10-point Visual Analogue Scale (VAS) immediately after the first local anaesthetic infiltration | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Immediate adverse events (allergic reactions, vasovagal response, unusual sensations) recorded at the time of infiltration 2. Perioperative complications (infection, bleeding, neurovascular injury) recorded during and after PNA 3. Correlation between injection pain and patient demographic variables (age, sex, comorbidities) and disease severity (Tubiana grade) using Spearman’s correlation coefficients | — |
Countries
Australia