Topical Green Tea Ointment in Treatment of Superficial Skin Cancer
Lykilorð
Útdráttur
Dagsetningar
Síðast staðfest: | 05/31/2015 |
Fyrst lagt fram: | 12/17/2013 |
Áætluð skráning lögð fram: | 01/05/2014 |
Fyrst sent: | 01/06/2014 |
Síðasta uppfærsla lögð fram: | 05/16/2016 |
Síðasta uppfærsla sett upp: | 05/17/2016 |
Raunverulegur upphafsdagur náms: | 10/31/2014 |
Áætlaður aðallokunardagur: | 08/31/2015 |
Áætlaður dagsetningu rannsóknar: | 01/31/2016 |
Ástand eða sjúkdómur
Íhlutun / meðferð
Drug: Sinecatechins 10%
Drug: Placebo
Stig
Armhópar
Armur | Íhlutun / meðferð |
---|---|
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. |
Hæfniskröfur
Aldur hæfur til náms | 18 Years Til 18 Years |
Kyn sem eru hæf til náms | All |
Tekur við heilbrigðum sjálfboðaliðum | Já |
Viðmið | 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 |
Útkoma
Aðal niðurstöður ráðstafanir
1. Percentage of patients with complete histological clearance [After 6 weeks treatment]
Aðgerðir vegna aukaatriða
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]