[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100620571":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":25,"locations":18,"responsibleParty":31,"collaborators":18,"id":33,"slug":34,"hasResults":35,"nctId":36,"briefTitle":37,"officialTitle":37,"acronym":38,"eligibilityCriteria":39,"healthyVolunteers":40,"sex":41,"minAge":42,"maxAge":18,"enrollmentInfo":43,"targetDuration":18,"studyType":46,"phases":47,"briefSummary":49,"conditions":50,"keywords":56,"overallStatus":66,"whyStopped":18,"lastUpdateSubmitDate":67,"lastUpdatePostDateStruct":68,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":18},{"fullName":5,"class":6},"AdventHealth","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Cosmetic Group (Laser\u002FBBL Therapy)","EXPERIMENTAL","Participants in this group will receive three sessions of ProFractional laser and\u002For Broadband Light (BBL) therapy following their qualifying body-contouring surgical procedure. Treatments will begin approximately 4 weeks postoperatively, with subsequent sessions at 8 weeks and 14 weeks (±2 weeks).\n\nLaser parameters will be determined by the treating provider based on clinical assessment and Fitzpatrick Skin Type.\n\nAssessments will include standardized scar photographs, SCAR-Q, and POSAS questionnaires at each visit and at 6 months postoperatively.\n\nThe objective is to determine whether early adjuvant energy-based therapy improves scar quality, appearance, and patient-reported satisfaction compared to standard care.",[13],"Device: ProFractional Laser Therapy and\u002For Broadband Light (BBL) Treatment",{"label":15,"type":16,"description":17,"interventionNames":18},"Non-Cosmetic Group (Standard Postoperative Care)","NO_INTERVENTION","Participants in this group will undergo standard postoperative wound management without laser or BBL therapy.\n\nThey will complete the same follow-up visits and outcome assessments as the cosmetic group-including SCAR-Q and POSAS questionnaires, and standardized photographic documentation-at 4, 8, and 14 weeks, and 6 months postoperatively.\n\nThis group serves as a comparator to evaluate the natural progression of scar healing and satisfaction under standard care conditions.",null,[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":18},"DEVICE","ProFractional Laser Therapy and\u002For Broadband Light (BBL) Treatment","ProFractional laser creates microthermal injury zones that stimulate collagen remodeling and accelerate re-epithelialization.\n\nBroadband Light (BBL) therapy uses filtered pulsed light to target hemoglobin and melanin, reducing erythema and pigmentation while promoting dermal repair.\n\nEach participant in the cosmetic arm will receive up to three sessions spaced 4-6 weeks apart, using device settings individualized by the investigator to the participant's scar characteristics and skin type.\n\nAll treatments are performed by trained and credentialed clinical staff in accordance with manufacturer safety guidelines and AdventHealth institutional standards.",[9],[26],{"name":27,"role":28,"phone":29,"phoneExt":18,"email":30},"Bridget Clinical Operations Manager, MS, MPH, CCRC, CCRP, PMP","CONTACT","407-303-5503","bridget.miller@adventhealth.com",{"type":32,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR","100620571","surgical-care-and-recovery-with-laser-evaluation-trial-scarlet-100620571",false,"NCT07359352","Surgical Care And Recovery With Laser Evaluation Trial (SCARLET)","SCARLET","Inclusion Criteria:\n\nAdults aged 18 years or older.\n\nScheduled to undergo one or more of the following major body-contouring procedures during the study period:\n\nBrachioplasty (arm lift)\n\nChest or breast contouring surgery\n\nAbdominoplasty or panniculectomy\n\nButtock lift or lower body lift\n\nThighplasty (thigh lift)\n\nAble and willing to provide written informed consent.\n\nAble to read and write in English (required for completion of validated questionnaires).\n\nWilling and able to comply with scheduled follow-up visits, questionnaires, and study procedures for up to 12 months post-surgery.\n\nExclusion Criteria:\n\nInability or unwillingness to provide informed consent.\n\nInability to comply with study visits or procedures.\n\nNon-English speakers, as the validated SCAR-Q and POSAS instruments are not currently available in equivalent translations.\n\nCurrent use of nicotine or nicotine-containing products, including cigarettes, vaping, chewing tobacco, or nicotine replacement therapy, due to the known adverse effects of nicotine on wound healing and scar formation.\n\nAny medical condition, treatment, or circumstance that, in the opinion of the Investigator, may increase participant risk, compromise safety, or interfere with study participation or data integrity.\n\nPregnant or breastfeeding women (laser\u002FBBL therapy contraindicated in pregnancy).\n\nHistory of abnormal scar formation such as keloids or hypertrophic scarring (if deemed clinically significant by the investigator).\n\nRecent energy-based treatment (laser, IPL, or BBL) to the surgical site within the previous 3 months.",true,"ALL","18 Years",{"count":44,"type":45},150,"ESTIMATED","INTERVENTIONAL",[48],"NA","The Surgical Care and Recovery with Laser Evaluation Trial (S.C.A.R.L.E.T.) is a prospective, single-center clinical study conducted at AdventHealth Medical Group Plastic and Reconstructive Surgery at Innovation Tower. The study evaluates whether early adjuvant ProFractional laser and\u002For Broadband Light (BBL) therapy improves the appearance, texture, and patient-reported outcomes of surgical scars following major body-contouring procedures. Participants undergoing qualifying surgeries will be grouped as either cosmetic (receiving three laser\u002FBBL sessions) or non-cosmetic (receiving standard care only). Scar outcomes will be assessed using validated instruments-SCAR-Q and Patient and Observer Scar Assessment Scale (POSAS)-along with standardized photographic analysis at serial follow-ups through six months postoperatively.",[51,52,53,54,55],"Post-surgical Scars","Hypertrophic Scars","Scar Appearance Dissatisfaction","Aesthetic Surgical Outcomes","Wound Healing After Body-contouring Surgery",[57,58,59,60,61,62,63,64,65],"Surgical scar","Postoperative scar","Hypertrophic scar","Body-contouring surgery","Abdominoplasty scar","Brachioplasty scar","Thighplasty scar","Scar revision","Laser-assisted scar remodeling","NOT_YET_RECRUITING","2026-01-14",{"date":69,"type":70},"2026-01-22","ACTUAL",{"date":72,"type":45},"2026-04-01",{"date":74,"type":45},"2027-10-01",{"name":5,"class":6}]