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A Pilot Study of the Treatment of Facial Nodular and Nodulocystic Basal Cell Carcinoma With Double Curettage and Cautery Followed by Application of Imiquimod to the Base

A Pilot Study of the Treatment of Facial Nodular and Nodulocystic Basal Cell Carcinoma With Double Curettage and Cautery Followed by Application of Imiquimod to the Base

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00463359
Enrollment
50
Registered
2007-04-20
Start date
Unknown
Completion date
Unknown
Last updated
2007-04-20

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

Conditions

Basal Cell Carcinoma

Keywords

basal cell carcinoma, curettage, Imiquimod, treatment

Brief summary

The purpose of this study is to determine recurrence rates of nodular Basal Cell Carcinomas on the face removed with curettage and electrodessication (cautery) followed by application of Imiquimod cream to the base and further to achieve lower recurrence rates than after treatment with curettage and electrodessication alone.

Detailed description

Basal Cell Carcinomas (BCC) are the commonest form of skin cancer in the white population. The face is where they most frequently occur and the nodular BCCs are the commonest type. Curettage and cautery/electrodessication (C&C) has been an established way of management of nodular BCCs for years, being a simple surgical procedure readily performed in outpatient clinics with good aesthetic results and high cure rates. The purpose of this study is to determine recurrence rates of nodular BCCs on the face removed with C&C followed by application of Imiquimod cream to the base and further to achieve lower recurrence rates than after treatment with C&C alone. Imiquimod is an immune response modifier with anti-tumour effects already licensed for the treatment of superficial BCCs in the UK.

Interventions

PROCEDUREcurettage and cautery

Sponsors

NHS Greater Glasgow and Clyde
CollaboratorOTHER
Glasgow Western Infirmary
CollaboratorOTHER
University of Glasgow
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
49 Years to 89 Years
Healthy volunteers
Yes

Inclusion criteria

* Well-defined primary, not previously treated nodulo-cystic BCC * Size of the lesions: ≤ 1cm diameter * Facial lesions * Patient compliance competent * Patient physically able to apply the treatment (cream)

Exclusion criteria

* Recurrent lesions * Superficial, morphoeic or pigmented BCC * Lesions close to vital structures; i.e. where C&C is not considered a standard treatment (eyelids, inner canthus, free borders) * Lesions within 1 cm of the eyelids, nose, lips and hairline * Immunosuppressed patients * Women in childbearing age, pregnancy and breast-feeding * Ages \<50 or \>90 * Patients compliance incompetent * Patients physically incapable to apply the treatment (cream) * Patients with Gorlin Syndrome (nevoid Basal Cell Carcinoma syndrome)

Design outcomes

Primary

MeasureTime frame
Basal Cell Carcinoma recurrence rates in 3 years

Countries

United Kingdom

Contacts

Primary ContactRobert Herd, Consultant Dermatologist
robert.herd@northglasgow.scot.nhs.uk+441412111000

Outcome results

None listed

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