The objective of the study is to compare pain reduction and disability reduction in two groups of patients diagnosed with de Quervain syndrome who will undergo ultrasound-guided infiltrative treatment with corticosteroid as per normal clinical practice: * the control group will subsequently be subjected to a standard treatment based on the European guidelines of the HANDGUIDE group, * the experimental group will subsequently carry out a program of eccentric exercises.
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Numeric Pain Rating Scale
Timeframe: At baseline (day 0)
Numeric Pain Rating Scale
Timeframe: After 1 month
Numeric Pain Rating Scale
Timeframe: After 3 months
Numeric Pain Rating Scale
Timeframe: After 6 months