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Clinical Trials in Egypt / NCT07306130
Enrolling by invitation Observational

Consensus on Skin Care in Breast Cancer Patients

NCT07306130 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-11-01
Last updated
2025-12-29

Condition(s) studied

RejuvenationSkin Care DermocosmeticsBreast Cancer

Study summary

Skin toxicity is one of the most common and impactful adverse effects of breast cancer treatment, affecting patients undergoing chemotherapy, targeted therapies, endocrine therapy, and radiotherapy. Current research and expert consensus highlight the importance of early, preventive, and gentle skin-care regimens to preserve barrier function and reduce treatment interruptions. Evidence supports the use of mild, fragrance-free cleansers, twice-daily emollient moisturization, and consistent broad-spectrum photoprotection throughout therapy. For radiation dermatitis, studies show that prophylactic moisturizers, silicone- or hydrofilm-based dressings, and short-course topical corticosteroids significantly reduce severity. Targeted therapies, particularly EGFR/HER2 inhibitors, require anticipatory management with barrier repair, topical anti-inflammatory agents, and oral antibiotics when papulopustular eruptions develop. Dermocosmetic products designed for sensitive or oncology-treated skin have demonstrated improvements in symptom burden and quality of life. Overall, the consensus emphasizes patient education, avoidance of irritants, multidisciplinary dermatologic-oncologic collaboration, and proactive rather than reactive care to effectively mitigate skin-related adverse events in breast cancer patients.

Eligibility

Sex
ALL
Min age
25 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: * Clinical Expertise: Must be a practicing healthcare professional (HCP) with a minimum of \[e.g., 5-10\] years of clinical experience in breast cancer management, supportive care, or oncology-related dermatology. * Geographic and Practice Diversity: Representation from different geographical regions and practice settings (e.g., academic centers, community hospitals) to ensure broad applicability of the recommendations. Availability and Willingness to Participate: Must formally agree to commit to the entire multi-round Delphi process (typically 2-4 rounds) within the specified timeline. Exclusion Criteria: * Inability or unwillingness to complete Delphi rounds. * Lack of clinical experience with breast cancer patients. * Industry representatives without direct clinical practice.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Venus Research Center Cairo Egypt

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07306130 on ClinicalTrials.gov ↗ ← All trials in Egypt