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Very Low Frequency Magnetic Fields Versus the Supplement Xinepa in the Treatment of the Carpal Tunnel Syndrome

Effectiveness of Very Low Frequency Magnetic Fields Versus the Supplement Xinepa in the Treatment of the Carpal Tunnel Syndrome: Randomized Double-blind Controlled Clinical Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02891512
Enrollment
31
Registered
2016-09-07
Start date
2015-07-31
Completion date
2016-01-31
Last updated
2016-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carpal Tunnel Syndrome

Keywords

Magnetic Fields, Pain, Paresthesia, Visual Analogue Scale

Brief summary

The purpose of the study is to determine the effectiveness of the treatment with very low frequency magnetic fields (ELF) on the reduction of pain and the relief of the associated signs such as sensitivity disorders that affect the first three fingers and half of the fourth finger of the hand in patients with carpal tunnel syndrome versus the supplement (= Xinepa).

Interventions

OTHERELF

Very low frequency magnetic fields (ELF) at intensity of 100 mT and a frequency of 1-80 Hz. Protocol (antiedema-antinflammatory): 12 sessions, 3 times a week for 4 consecutive weeks, each session lasted 30 minutes.

OTHERXinepa®

2 tablets of Xinepa daily (morning and evening) for 1 month.

OTHERPlacebo Xinepa®

2 tablets of Xinepa placebo daily (morning and evening) for 1 month.

Sponsors

University of Roma La Sapienza
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis of carpal tunnel syndrome

Exclusion criteria

* Pregnancy; * Pacemaker or other metallic implants; * Systemic infectious disorders; * Neoplastic disorders; * Epilepsy; * Severe heart disease. * Known hypersensitivity to the components of Xinepa

Design outcomes

Primary

MeasureTime frameDescription
Change of Visual Analogue Scale (VAS) from baseline to 12 weeksbaseline, 4 weeks, 12 weeksIt is a scale for the assessment of pain and it's based on a ten point scale, where 0 means no pain and 10 the greatest pain ever both at rest and during movements.

Secondary

MeasureTime frameDescription
Change of Semmes-Weinstein Monofilaments of light touch and pressure sensation test from baseline to 12 weeksbaseline, 4 weeks, 12 weeksInvolves the use of five monofilaments of different colours that identify the levels of decrease in sensitivity, measurable, necessary for the evaluation of the perception of the surface touch.
Change of Boston Carpal Tunnel Questionnaire from baseline to 12 weeksbaseline, 4 weeks, 12 weeksIt consists of two scales, the scale of the severity of symptoms (SSS) and functional status scale (FSS). The first includes the first 11 questions relating to: the intensity of pain during the day and night, lasting pain during the day, sleep, weakness, tingling sensation during the night and its frequency and abilities. Each question provides a metric scale ranging from 1 (absence of symptoms) to 5 (severe symptoms). The second scale includes the last eight questions concerning activities such as writing, buttoning clothes, hold a book while reading, hold up the phone, clean, carry bags, open the lid of a jar.
Change of the measurement of the grip strength trough the Jamar dynamometer from baseline to 12 weeksbaseline, 4 weeks, 12 weeksIt consists of a manometer with a double scale to recorder static force in kilos and pounds and a handle with 5 different positions of increasing amplitude from 3.5 cm to 8.8 cm. The patient holds the dynamometer and performs a grip at maximum force. The final score originates from the average of three measurements taken for each position of the handle.
Change of the measurement of the pinch strength trough the Pinch Gauges dynamometer from baseline to 12 weeksbaseline, 4 weeks, 12 weeksIt consists of a manometer with a double scale to recorder static force in kilos and libbre and two caliper levers with the tips away from each other of 2.2 cm/ 1.9 cm. Three types of pliers are evaluated: side, three tips, tip against tip. The patient holds the dynamometer and performs a grip at maximum force. The final score originates from the average of three measurements taken for each type of tongs.
Change of electroneurography from baseline to 12 monthsbaseline, 4 weeks, 12 weeksIt allows the study of nerve of the median nerve (speed of motor-sentitive run and latency).

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026