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Reflectance Confocal Microscopy to Diagnose MM & LM

Reflectance Confocal Microscopy to Diagnose Malignant Melanoma and Lentigo Maligna

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03508297
Enrollment
597
Registered
2018-04-25
Start date
2017-03-14
Completion date
2020-08-31
Last updated
2021-11-12

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

Conditions

Lentigo Maligna, Melanoma (Skin)

Keywords

Confocal, RCM, Imaging, Skin cancer

Brief summary

A reflectance confocal microscope is a machine which is able to examine the upper layers of the skin painlessly and without the need for taking a biopsy. We would like to examine the images taken by the confocal microscope to see if it can help more accurately identify lesions which are worrying rather than a benign mole. We are performing this study in patients in whom we have recommended excising a mole to exclude a cancer. If the results of the study show that the confocal microscope can help more accurately diagnose Melanomas then this would reduce the number of biopsies that are taken that turn out not to be cancerous (ie unnecessary biopsies).

Detailed description

Study Design This is an observational, non-randomised, non-controlled, prospective cohort study to look at the efficacy of in vivo RCM as a diagnostic tool in the diagnosis of MM and LM. Study Endpoints The hypothesis of this study is that the use of RCM is would reduce the NNE prior to definitive treatment by at least 30% from the current value of approximately 10. The secondary hypothesis is that the intra- & inter-observer agreement for interpreting the RCM images will have kappa scores 0.6 or greater (indicating good agreement). Setting and recruitment Patients will be recruited from the outpatient clinics of the Skin Care Network Barnet, and from the outpatient clinics of the Chase Farm and Barnet sites of Royal Free Hospital NHS Foundation Trust. Participants The number of true negative lesions examined in this study will be 654. It is anticipated that this will result in a total of 661 lesions being recruited. 10% of participants are expected to have more than one lesion sampled. The result of biopsy for each lesion will not be known until after the lesion has been included in the study. Therefore lesions will be added to the study until the required number of true negatives has been included.

Interventions

DIAGNOSTIC_TESTIn-vivo imaging

Skin cancer is imaged using RCM and a diagnosis is recorded before patient is returned to standard of care (biopsy).

Sponsors

Skin Care Network Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

1. Age 18 years or older 2. Patient with a pigmented lesion recommended for excision because of suspicion of MM or LM. 3. Patient willing and able to give informed consent

Exclusion criteria

1. Recurrent MM or LM 2. Patient on immunosuppresants 3. Patient with significant co-morbidity or skin disease 4. Patient not suitable for diagnostic biopsy 5. Location of lesion unsuitable, inaccessible or impractical for scanning with RCM as determined by investigator

Design outcomes

Primary

MeasureTime frameDescription
Number Needed to ExciseDuring exam (biopsy results typically available within one week).The number of suspicious lesions (defined by conventional histology) biopsied to find one cancerous lesion

Secondary

MeasureTime frameDescription
intra- & inter-observer agreement for interpreting the RCM images will have kappa scores 0.6 or greater6 monthsA measure of how consistently readers can diagnose from confocal images.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026