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Effectiveness of leech therapy in epicondylitis humeroradialis - a randomized controlled trial - leeches in epicondylitis

Effectiveness of leech therapy in epicondylitis humeroradialis - a randomized controlled trial - leeches in epicondylitis

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2005-000893-27-DE
Enrollment
Unknown
Registered
2005-04-14
Start date
2005-09-02
Completion date
Unknown
Last updated
2012-03-19

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

Conditions

In the planned study patients with painful epicondylitis humeroradialis of the ellbow are treated with leeches or a standard treatment.

Interventions

Trade Name: natural leech Product Name: leech (Hirudo medicinalis), lively Pharmaceutical Form: Trade Name: Voltaren Emulgel Pharmaceutical Form:

Sponsors

Prof. Gustav Dobos, Kliniken Essen Mitte
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Diagnosis of Epicondylitis - pain on more than 50% of the days in the last month - age 20-75 years old - informed consent - no planned treatment or operation within the next 3 month Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria: - other causes of ellbow pain than epicondylitis humeroradialis - steroid injection within the last 3 weeks - hemophilia or othe bleeding disorders - medication with marumar, warfarin, heparin or heparinoids - anemia - renal failure - severe other comorbidity - pregnancy - psychosis - dementia

Design outcomes

Primary

MeasureTime frame
Main Objective: Background: Leeches therapy has been proven to be successful in the treatment of knee osteoarthritis. Its effects in epicondylitis is unknown. Main objective: To evaluate the symptomatic effects of a single leech therapy versus topical adminstration of diclofenac at epicondylitis humeroradialis. Main outomce parameter is assessed by Visual Analogue scale for pain at one week after the intervention.;Secondary Objective: To assess the improvement of Joint function (DASH-Questionaire), related qualitiy of life (SF 36) and isometric strength of the hand extensors.;Primary end point(s): Pain reduction on self rated VAS sum-score at day 7 after the intervetion compared to baseline.

Countries

Germany

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026