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De Quervain's Disease in the Acute Phase:a Study Aimed at Evaluating the Effectiveness of Standard Physiotherapy Treatment (HANDGUIDE), Compared to Experimental Treatment After Performing Ultrasound-guided Infiltrative Therapy.

I

Istituto Ortopedico Rizzoli

Status

Enrolling

Conditions

De Quervain Disease
Hand Tenosynovitis

Treatments

Other: Rehabilitation
Other: Standard

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

134 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients of both sexes with a minimum age of 18 years;
  • Medical diagnosis of de Quervain syndrome assessed through orthopedic clinical examination e confirmation by ultrasound;
  • Signing of the informed consent and participation in the study.

Exclusion criteria

  • Patients who are not self-sufficient or not able to understand and want;
  • Presence of other pathologies in the hand affected by de Quervain pathology, such as intersection syndrome, neuropathies, fractures, rhizoarthrosis, arthrosis of the radio-carpal or intercarpal joint, intercarpal instability, cervical radiculopathy, rheumatic or metabolic pathologies;
  • Pregnant or breastfeeding women.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

134 participants in 2 patient groups

Standard
Active Comparator group
Treatment:
Other: Standard
Experimental
Experimental group
Treatment:
Other: Rehabilitation

Trial contacts and locations

1

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Central trial contact

Fabio Vita, MD; Federico Pilla, MD

Data sourced from clinicaltrials.gov

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