Stanford Health Care: Supportive Dermato-Oncology Program
Palo Alto, California, 94304, United States
Location contact
Hannah Clinical Research Coordinator
CONTACT
Lisa Zaba, MD, PhD
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07767448
The goal of this clinical trial is to evaluate whether cosmeceutical topical moisturizers can help with skin dryness in participants with cancer experiencing a dermatological adverse event from cancer therapies. The main question it aims to answer is:
Does cosmeceutical topical moisturizers help with skin dryness?
Participants will:
* Visit the clinic for a baseline visit to complete skin evaluation and tests. * Apply cosmeceutical topical moisturizers daily from baseline up until the follow-up visit. * Visit the clinic for a follow-up visit (approximately 2-4 weeks from baseline) for a repeat skin evaluation and tests.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Palo Alto, California, 94304, United States
Hannah Clinical Research Coordinator
CONTACT
Lisa Zaba, MD, PhD
PRINCIPAL_INVESTIGATOR
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Moisturizer wash applied once in the morning and once in the evening.
Moisturizer applied once in the morning and once in the evening.
Balm applied once in the morning and once in the evening.
Time frame: From baseline visit to follow-up visit (approximately 2-4 weeks).
Change in patient-reported skin dryness severity from baseline to follow-up visit (2-4 weeks) as measured by validated dryness severity scale (0-10 numerical rating scale where 0 = no dryness and 10 = severe dryness).
Time frame: From baseline visit to follow-up visit (2-4 weeks).
The time from baseline to the first documented improvement in dryness symptoms, defined as either a ≥2-point reduction in dryness severity score from baseline or patient-reported meaningful improvement in dryness symptoms, whichever occurs first. Lower values indicate a faster improvement in symptoms.
Time frame: From baseline visit to follow-up visit (2-4 weeks).
Change in skin hydration from baseline to follow-up, measured using corneometry and reported in corneometry units (CU). Higher corneometry values indicate greater stratum corneum hydration. Positive changes from baseline reflect improved skin hydration, whereas negative changes indicate reduced hydration.
Time frame: From baseline visit to follow-up visit (2-4 weeks).
Change in skin barrier function from baseline to follow-up, measured by transepidermal water loss (TEWL) and reported in g/h/m². TEWL quantifies the amount of water that passively evaporates through the skin. Lower TEWL values indicate improved skin barrier integrity and reduced water loss, while higher values indicate increased barrier disruption. Negative changes from baseline reflect improvement, whereas positive changes indicate worsening skin barrier function.
Contact information is provided by the study sponsor or research team.
Stanford University
Other
Characterization of Skin Changes (Clinical, Physiological and Pathological) Leading to Dermatological Adverse Events From Chemotherapy, Targeted Therapy, Hormonal Therapy, and Immune Checkpoint Inhibitors
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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