Hair Regrowth Following Partial Thickness Stages in Mohs Micrographic Surgery of Squamous Cell Carcinoma in Situ: A Prospective Pilot Study
| Registry | NCT07809191 |
|---|---|
| Status | Not yet recruiting |
| Phase | Not applicable |
| Study type | Interventional; na, single group, masking: none, prevention |
| Enrollment | 15 (Estimated) |
| Sponsor | The Cooper Health System (Other) |
| Conditions | Squamous Cell Carcinoma (Skin), Squamous Cell Carcinoma in Situ, Alopecia |
| Interventions | Partial Thickness Excision (Procedure) |
| Dates | start 2026-09-01 (estimated), primary completion 2027-07-17 (estimated), completion 2028-07-17 (estimated), first posted 2026-09-09, last updated 2026-09-09 |
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All trials for Squamous Cell Carcinoma (Skin) All trials for Squamous Cell Carcinoma in Situ All trials of Partial Thickness Excision
Participants are being approached to participate in this study because they are undergoing surgery for a skin cancer known as squamous cell carcinoma in situ (SCCIS) on the scalp. Standard surgical techniques may remove deeper structures that contain hair follicles, which can result in permanent hair loss. This study evaluates whether a modified surgical technique, known as partial thickness excision, can preserve hair growth and improve cosmetic outcomes. Participation involves minimal risk beyond the standard risks of Mohs surgery. If patients choose to participate, their surgery will be performed using this technique, and photographs will be taken over time to evaluate hair regrowth and healing.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| Partial Thickness Excision | Experimental | Procedure: Partial Thickness Excision | Participants will receive excision of their squamous cell carcinoma in situ of the scalp via partial thickness excision (removal of epidermal and superficial dermal tissue) in an effort to preserve hair follicles and hair growth potential. |
Sex: All, ages: 18 Years to any
Inclusion Criteria: * Adults ≥ 18 years old * Histologically confirmed SCCIS * Lesions located in the hair-bearing scalp * Ability to provide informed consent Exclusion Criteria: * Invasive, poorly differentiated, or high-risk SCC features (e.g., perineural invasion) * Recurrent SCC at the same site * Prior radiation therapy to the scalp * Scarring alopecia or active inflammatory scalp disease at the treatment site * Immunosuppression that, in the investigator's judgement, increases oncologic risk * Use of topical minoxidil, oral minoxidil, finasteride, spironolactone, or other hair-growth promoting agents