Effect of Topical Application of Hypertonic Saline on Melanoma on Its Sizes and Number.
Melanoma (Skin)
About this trial
This is an interventional treatment trial for Melanoma (Skin)
Eligibility Criteria
Inclusion Criteria: Patients with clinically-confirmed Melanoma (any location and any stage) who have poorly responded to at least one cycle of conventional and standard therapy (Chemotherapy, Radiation or Drug therapy). Age 5 to 80 years old Life expectancy of at least 1 year Can understand and read English Lives in USA. Patient who do not meet the Inclusion Criteria but still wish to participate will be accepted as Observational participants, but their Melanoma measurements will be not be taken into account when analyzing the Study statistically. Exclusion Criteria: Skin eczema and/or other skin conditions contraindicated to skin dehydration. Ulcers or open wounds close to Melanoma Any medical condition that might cause the patient to lose consciousness Participants who are not residents of USA.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
Active Group - Sodium Chloride Crystal Topical
Control Group - Plain Water topical application
Each patient of the Active group will have their Melanoma covered by 2 drops of water, followed by applying Sodium Chloride granules to saturate the melanoma surface then add 2 more drops of water, then cover the NaCl-granules-covered Melanoma with a bandage. The bandage will stay in place for 12 hours daily and the procedure will be repeated daily for a total of 7 consecutive days, in addition to their standard treatments they receive from their health care providers, if any.
Each patient of the Control group will have their Melanoma covered by 4 drops of water, then covered by a bandage. The bandage will stay in place for 12 hours daily and the procedure will be repeated daily for a total of 7 consecutive days, in addition to their standard treatments they receive from their health care providers, if any.