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Clinical Trial Summary

The purpose of this study is to determine if topical imiquimod is effective in the pathological complete regression of lentigo maligna.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01161888
Study type Interventional
Source University Hospital Birmingham NHS Foundation Trust
Contact
Status Completed
Phase Phase 4
Start date June 2010
Completion date March 2012

See also
  Status Clinical Trial Phase
Completed NCT06046144 - Comparison of 3 in Vivo Microscopic Imaging Techniques for the Diagnosis of Pigmented Tumors
Completed NCT00707174 - Combination Therapy With Imiquimod Cream 5% and Tazarotene Cream 0.1% for the Treatment of Lentigo Maligna N/A
Completed NCT03508297 - Reflectance Confocal Microscopy to Diagnose MM & LM
Withdrawn NCT02306512 - Mohs and Immunofluorescence for Malignant Melanoma In Situ N/A
Completed NCT02723721 - Prospective Study of Ingenol Mebutate for Non-invasive Lentigo Melanoma of the Face Phase 2
Terminated NCT04688749 - Use of Electrical Impedance Spectroscopy (EIS) for Early Diagnosis of Skin Damage
Active, not recruiting NCT01088737 - Imiquimod to Detect Residual Lesions and Prevent Recurrence of Lentigo Maligna Phase 2/Phase 3
Completed NCT02685592 - Photodynamic Therapy for Lentigo Maligna Using 5-aminolevulinic Acid Nanoemulsion as a Light Sensitizing Cream Phase 4
Completed NCT02394132 - Radiotherapy or Imiquimod in Complex Lentigo Maligna Phase 3
Completed NCT00785369 - In Vivo Confocal Microscopy for Pigmented Lesion Diagnosis N/A
Recruiting NCT06014619 - Complications and Recurrences After Mohs Micrographic Surgery and Slow Mohs