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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06399484
Other study ID # PI23/437
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 15, 2024
Est. completion date December 15, 2024

Study information

Verified date May 2024
Source Universidad de Zaragoza
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 30
Est. completion date December 15, 2024
Est. primary completion date September 15, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Manual mobilizations of the median nerve
Slippage of the median nerve in the wrist: the subject's starting position (P0) will be recumbent supine with the cervical spine in a neutral position, the shoulder girdle in neutral position, 30º of glenohumeral abduction in neutral rotation, 90º of elbow flexion, prone-supination of the neutral forearm, wrist and fingers in neutral position. From this position the movements will be 1) Glenohumeral abduction up to 90º; 2) Glenohumeral external rotation to the frontal plane; 3) Supination of the forearm; 4) Extension of the wrist and fingers; 5) Elbow extension. This position is will combine with an ipsilateral cervical inclination (distal sliding). The proximal slide is carried out bringing the fingers of the hand towards the flexion while performing a contralateral cervical tilt. Median nerve tension: the starting position and movements are the same described above but this time it will be done with contralateral cervical tilt.
Wrist movements
Movements of the wrist joint will be performed as a placebo treatment

Locations

Country Name City State
Spain Hospital Clínico Universitario Lozano Blesa Zaragoza

Sponsors (1)

Lead Sponsor Collaborator
Universidad de Zaragoza

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Distal motor latency (APB) (ms) Before and immediately after the intervention
Primary Motor amplitude (APB) (mV) Before and immediately after the intervention
Primary Median motor velocity (m/s) Before and immediately after the intervention
Primary Median sensory conduction (digit II) (13 cm) (m/sec) Before and immediately after the intervention
Primary Sensory amplitude (µV) Before and immediately after the intervention
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