Topical Green Tea Ointment in Treatment of Superficial Skin Cancer
Märksõnad
Abstraktne
Kuupäevad
Viimati kinnitatud: | 05/31/2015 |
Esmalt esitatud: | 12/17/2013 |
Hinnanguline registreerumine on esitatud: | 01/05/2014 |
Esmalt postitatud: | 01/06/2014 |
Viimane värskendus on esitatud: | 05/16/2016 |
Viimati värskendus postitatud: | 05/17/2016 |
Õppe tegelik alguskuupäev: | 10/31/2014 |
Eeldatav esmane lõpetamise kuupäev: | 08/31/2015 |
Eeldatav uuringu lõpetamise kuupäev: | 01/31/2016 |
Seisund või haigus
Sekkumine / ravi
Drug: Sinecatechins 10%
Drug: Placebo
Faas
Käerühmad
Arm | Sekkumine / ravi |
---|---|
Experimental: Sinecatechins 10% Patients are instructed to apply a thin layer of the sinecatechins 10% ointment twice daily (morning and evening) in a thin layer to the tumour including 5mm of the surrounding skin. Before applying a new layer patients are advised to wipe off the remnants. Sinecatechins 10% ointment has to be applied for six weeks. Patients are advised to wash their hands after each application to prevent spreading of the ointment. | Drug: Sinecatechins 10% |
Placebo Comparator: Placebo Patients are instructed to apply a thin layer of the placebo ointment twice daily (morning and evening) in a thin layer to the tumour including 5mm of the surrounding skin. Before applying a new layer patients are advised to wipe off the remnants. Sinecatechins 10% ointment has to be applied for six weeks. Patients are advised to wash their hands after each application to prevent spreading of the ointment. | Drug: Placebo Composition, apart from the active substance, is otherwise identical to the investigational medical product. |
Abikõlblikkuse kriteeriumid
Õppimiseks sobivad vanused | 18 Years To 18 Years |
Uuringuks kõlblikud sood | All |
Võtab vastu tervislikke vabatahtlikke | Jah |
Kriteeriumid | Inclusion Criteria: - Adults aged 18 years or older - Primary histological proven superficial basal cell carcinoma ≥ 4mm and ≤ 20mm - Comorbidities may not interfere with study treatment (evaluated by investigator) - Capable to understand instructions Exclusion Criteria: - Recurrent sBCC (previous treatment) - Breast-feeding or pregnant women - Serious comorbidities - Use of immunosuppressive medication during the trial period or within 30 days before enrolment - Patients with genetic skin cancer disorders - Tumour located in the H zone (high-risk area of face) or scalp |
Tulemus
Esmased tulemusnäitajad
1. Percentage of patients with complete histological clearance [After 6 weeks treatment]
Sekundaarsed tulemusmõõdud
1. Number of applications actually done by the patient divided by the total prescribed number of applications. [Week 6]
2. Number of local skin reactions, adverse events and serious adverse events [Up to 3 weeks]