Radial Pressure Wave Therapy With or Without Parameter Modulation for Carpal Tunnel Syndrome.
60 patients around the world
Available in Mexico
This is a double-blind randomized controlled trial designed to explore the effects of
different dosing strategies of radial pressure wave therapy in patients with mild to
moderate carpal tunnel syndrome. Sixty patients aged 18 to 75 years, with clinical and
electrodiagnostic confirmation of CTS, will be recruited and randomly assigned (1:1) to
one of two intervention groups: (1) RPWT with constant parameters; or (2) RPWT with
modulated parameters (progressive variation of frequency and pressure during each
session). All participants will receive three weekly sessions of RPWT and follow a
standardized home-based exercise protocol for wrist and hand mobility.
The primary outcome will be the change in pain intensity, measured with the Visual Analog
Scale VAS. Secondary outcomes include functional status assessed with the Boston Carpal
Tunnel Questionnaire, grip strength using a calibrated hydraulic hand dynamometer, and
neurophysiological parameters such as sensory conduction velocity, distal motor latency,
and CMAP amplitude of the median nerve. Neurophysiological evaluations will be performed
using the Nicolet Viking Quest system following standardized protocols.
Assessments will take place at baseline, 2 months, and 4 months after treatment
initiation, except for electrodiagnostic studies which will be performed only at baseline
and at 4 months. Statistical analysis will include mixed-design repeated measures ANOVA
to assess intra- and inter-group effects and time-by-group interactions. The study
complies with ethical standards and good clinical practice guidelines.
Armando Tonatiuh Avila Garcia
1Research sites
60Patients around the world
This study is for people with
Mononeuropathies of the upper limb
Carpal tunnel syndrome
Requirements for the patient
To 75 Years
All Gender
Medical requirements
Adults aged 18 to 75 years.
Clinical diagnosis of carpal tunnel syndrome based on symptoms such as nocturnal paresthesia, numbness in the median nerve distribution, and/or thenar weakness.
At least one positive provocative test (e.g., Tinel's, Phalen's, or Durkan's test).
Symptoms present for at least 1 month.
NPRS (Numeric Pain Rating Scale) score ≥ 4 at baseline.
Able and willing to attend all intervention sessions and follow-up assessments.
Able to provide informed consent.
Prior wrist surgery on the affected side.
Prior treatment with radial pressure wave therapy for CTS.
Diagnosis of polyneuropathy, cervical radiculopathy, or systemic conditions affecting nerve function (e.g., uncontrolled diabetes, hypothyroidism, rheumatoid arthritis).
Severe thenar atrophy or muscle wasting.
Pacemaker or other implanted electronic devices.
Pregnancy.
Currently participating in another clinical trial or intervention study.
Inability to understand or complete the study procedures.
Sites
Hospital Civil de Guadalajara Fray Antonio Alcalde