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A randomized clinical trial of the effects of Tea tree essential oil on adult leg cellulitis of class II in the Eron/Dall classification system for cellulitis: Pilot study. - Tea tree and cellulitis

A randomized clinical trial of the effects of Tea tree essential oil on adult leg cellulitis of class II in the Eron/Dall classification system for cellulitis: Pilot study. - Tea tree and cellulitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2010-021842-23-IS
Enrollment
30
Registered
2010-07-30
Start date
2010-09-15
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

Cellulitis of the lower leg of adult patients that have been admitted to Landspitali University Hospital and are on iv antibiotics.

Interventions

Trade Name: Tea-Tree m.a. extra Pharmaceutical Form: Cutaneous liquid Pharmaceutical form of the placebo: Cutaneous liquid Route of administration of the placebo: Cutaneous use

Sponsors

University of Iceland
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. patient with cellulitis of class II in the Eron/Dall classification system for cellulitis 2. patient on iv antibiotics 3. patient who gets admitted to one of the general medicine wards 4. patient who writes and understands icelandic 5. patient who can give written and informed concent to participate in the clinical trial 6. patient admitted for at least six days or for the length of the treatment period 7. patient with no history of any allergies 8. patient who has not used any antibiotic, inflammatory or steroid cream on the diseased leg one day prior admission 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: 1. childbearing or lactating women 2. patient with HIV, hepatitis or canser 3. patient with COPD or has FEV1<80% or is taking inhalants 4. patient with impared kidney function or has GFR<60ml/min 5. patient with impaired memory, delerium or dementia 6. patient with psoriasis or stasis dermatitis

Design outcomes

Primary

MeasureTime frame
Main Objective: Is to test a new intervention against cellulitis. ;Secondary Objective: To observe if there are any complications of the new treatment.;Primary end point(s): 1. patient has finished five days of treatment with oil application to the leg and has finished all outcome measurements on day six and gotten some information/education from the researcher. The patient drops out of the clinical trial if: 1. patient is discharged to early 2. patient is discharged to a surgical department 3. patient gets any complication or adverse effects because of the new treatment 4. patient dies 5. patient desides to quit participating in the clinical trial 6. patient gets new diagnosis of diseases or any new symptoms

Countries

Iceland

Outcome results

None listed

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