In Patients With Carpal Tunnel Syndrome, Median Nerve Conduction is Evaluated After Nerve Mobilizations

University of Zaragoza

Status: Not yet enrolling

Conditions: Carpal Tunnel Syndrome

Treatments: Other: Wrist movements; Other: Manual mobilizations of the median nerve

Study type: Interventional

Funder types: Other

Identifiers

NCT06399484

PI23/437

Details and patient eligibility

About

This project is linked to the line of research on carpal tunnel syndrome, of the PhysiUZerapy research group, belonging to the University of Zaragoza. Within this line, the biomechanical and physiological effect of the proposed technique has been investigated, both in healthy subjects, in cadavers and in patients with carpal tunnel syndrome (CTS), resulting in the reading of 2 doctoral theses, the publication of 9 articles in high-impact journals. and the patent for a splint for the treatment of pathology. This project aims to provide information that is still lacking on the immediate effect of these techniques in patients with CTS. For this, there will be three groups of patients from the Lozano Blesa University Clinical Hospital distributed randomly. In two of the groups, sliding and neural tension techniques will be carried out (case group). The remaining group (control group) will be taken as a reference by performing a placebo treatment. Before and after carrying out these techniques, electrophysiological data will be collected to be able to compare them. This comparison is based on highlighting the differences between the data before the techniques and after, as well as between the case group and the control group.

Enrollment: 30 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Being over 18 years
• Present carpal tunnel syndrome diagnosed by electroneurogram
• Have understanding and communication skills
• Give consent to participate in the study

Exclusion criteria

• Have received previous surgery on the hand or wrist
• Present a severe limitation of movement in any of the joints of the affected upper limb
• Not signing the informed consent

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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30 participants in 2 patient groups, including a placebo group

Neural mobilization group

Experimental group

Description:

Manual mobilizations of the median nerve.

Treatment:

Other: Manual mobilizations of the median nerve

Placebo group

Placebo Comparator group

Description:

wrist movements no producing sliding of the median nerve

Treatment:

Other: Wrist movements