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Effectiveness of the "Tecaretherapy" in Patients With Lateral Elbow Tendinopathy

U

University of Liege

Status

Terminated

Conditions

Tendinopathy

Treatments

Other: CPT
Other: Active Tecaretherapy
Other: Inactive Tecaretherapy

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This RCT aims at investigating the effectiveness of the "Tecaretherapy" in patients with lateral elbow tendinopathy.

60 patients will be randomized into one of the following 3 groups:

  • "Conventional physiotherapy treatment (CPT)" (massage, eccentric exercises, stretching);
  • "CPT + Tecare" (idem CPT group + tecaretherapy during the eccentric exercises)
  • "CPT + Placebo Tecare" (idem "CPT + Tecare" group but with an inactive Tecare device) The treatment will include 18 30-minute sessions

Full description

This RCT aims at investigating the effectiveness of the "Tecaretherapy" in patients with lateral elbow tendinopathy.

60 patients will be randomized into one of the following 3 groups:

  • "Conventional physiotherapy treatment (CPT)" (massage, eccentric exercises by means of an isokinetic dynamometer, stretching);
  • "CPT + Tecare" (idem CPT group + Tecaretherapy during the eccentric exercises)
  • "CPT + Placebo Tecare" (idem "CPT + Tecare" group but with an inactive "Tecare" device) The treatment will include 18 30-minute sessions.

The "Tecaretherapy" consists in using a specific device providing high frequencies (between 300 kHz and 1 MHz) supposed to accelerate the tissues healing process.

Outcome sessions will be organized at baseline, after the first 9 sessions, at the end of the treatment as well as 3 and 6 months after the initial treatment session.

Enrollment

17 patients

Sex

All

Ages

18 to 55 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient suffering from a chronic lateral elbow tendinopathy confirmed by echography

Exclusion criteria

Patients:

  • with contra-indications for a Tecaretherapy (Pace maker, insuline pump, pregnancy, infection, fever, cancer, thrombophlebitis)
  • reporting injections and/or shockwaves in the past (for the tendinopathy)
  • with an associated neurogenic dysfunction

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

17 participants in 3 patient groups

"Conventional PT treatment (CPT)"
Other group
Description:
All treatment sessions include massage, eccentric exercises by means of an isokinetic dynamometer and stretching;
Treatment:
Other: CPT
"CPT + Tecare"
Experimental group
Description:
All treatment sessions include massage, eccentric exercises by means of an isokinetic dynamometer and stretching (idem CPT group). However, an active Tecaretherapy is also provided during the sessions
Treatment:
Other: Active Tecaretherapy
Other: CPT
"CPT + Placebo Tecare"
Sham Comparator group
Description:
All treatment sessions include massage, eccentric exercises by means of an isokinetic dynamometer and stretching (idem CPT group). However, an inactive Tecaretherapy is also provided during the sessions
Treatment:
Other: Inactive Tecaretherapy
Other: CPT

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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