Neurocutaneous Melanocytosis Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorMemorial Sloan Kettering Cancer Center

About this trial

This study will involve collecting information about the regular medical care you receive for large cutaneous melanocytic nevi (LCMN) or neurocutaneous melanocytosis (NCM).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Dark-colored patch of skin present at birth

Can be located anywhere on the individual's skin

May include satellite lesions

May be associated with hypertrichosis

Disqualifiers

Informed consent has not been provided.

Trial population

A target sample of 75 patients with LCMN and/or NCM will be enrolled in this registry study. The study is expected to accrue over ≥ 7 years. Currently, an estimated 50 LCMN patients are followed at MSK and we anticipate 25 or more to be referred from outside providers or from new patients seen at MSK. The patient population and the MSK referral base is growing at this time, making this enrollment goal as feasible.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 1 trial group
Group A: Neurocutaneous Melanocytosis

Trial outcomes

Primary outcomes

1

Collect retrospective and prospective clinical, treatment and outcome data about patients with Neurocutaneous Melanocytosis (NCM) worldwide

Time frame
Up to 7 years

Secondary outcomes

Other outcomes

Sponsors and contacts

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