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Influence of Microcurrent Parameters on Effectiveness in Treatment of Chronic Tennis Elbow

Influence of Microcurrent Parameters on Effectiveness of Treatment of Chronic Tennis Elbow - a Preliminary Trial

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00905736
Enrollment
24
Registered
2009-05-21
Start date
2009-04-30
Completion date
2009-12-31
Last updated
2010-06-22

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

Conditions

Tennis Elbow

Keywords

tendon, healing, microcurrent, chronic tennis elbow

Brief summary

Tennis elbow is a relatively common musculoskeletal disorder that can cause significant pain and disability. Treatment of the disorder is not always successful, and it often recurs or becomes chronic. More effective management options are required. There is evidence that electric microcurrent can promote tissue healing and symptom resolution in various chronic hard and soft tissue disorders, but few human studies have investigated its use with chronic tendon problems. It is an easily applied therapy with very few reports of side effects. It can be applied at home using a portable unit and, if it is clinically effective, may also prove more cost effective than other therapies. A clinical trial is planned to evaluate the therapy but, in the absence of relevant published evidence, a preliminary study is required to look for a treatment effect and inform a power calculation for sample size, The study is comparing the effects of two different forms of microcurrent treatment.

Interventions

PROCEDUREMicrocurrent treatment (controlled current)

primarily monophasic waveform of average amplitude 40 microamps, 1 hr daily for 3 weeks

PROCEDUREMicocurrent treatment (controlled voltage)

Microcurrent delivered for 6 hours daily for 3 weeks

Sponsors

University of Hertfordshire
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* symptoms of tennis elbow for at least 3 months * clinical diagnosis of tennis elbow

Exclusion criteria

* significant symptom improvement in previous month * receipt of any active treatment for the condition in the previous month * currently under the care of another health professional for tennis elbow * current cervical radiculopathy

Design outcomes

Primary

MeasureTime frame
Tissue healing as indicated by sonographybaseline, 3 weeks, 6 weeks, 4 months

Secondary

MeasureTime frame
Patient rating global changebaseline, 3 weeks, 6 weeks, 4 months
Pain free grip strengthbaseline, 3 weeks, 6 weeks, 4 months
Patient rated tennis elbow questionnairebaseline, 3 weeks, 6 weeks, 4 months
Adverse events3 weeks, 6 weeks, 4 months

Countries

United Kingdom

Outcome results

None listed

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