[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hair-thinning\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hair-thinning":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,74,107],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100643276","study-to-evaluate-xtress-gummy-supplement-in-men-with-androgenic-alopecia-100643276",false,"NCT07637071","Study to Evaluate Xtressé Gummy Supplement in Men With Androgenic Alopecia","Pilot Study to Evaluate the Efficacy and Safety of Xtressé™ Gummy-Based Nutraceutical Supplement in Men With Androgenic Alopecia","Inclusion Criteria:\n\n* Males aged 18-65\n* Norwood III to IV, vertex focused\n* Fitzpatrick skin type I to VI\n* Ability and willingness to comply with study protocol\n\nExclusion Criteria:\n\n* Change in other hair treatments in 3 months prior to study enrollment.\n* Known uncontrolled health conditions.\n* History of hair or scalp disorders that could interfere with study results.\n* History of metabolic syndrome.","MALE","18 Years","65 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this study is to determine how safe and effective it is to improve hair growth using an active gummy treatment in men with androgenic alopecia.\n\nThe main aims of this trial are:\n\n1. To confirm using photographic analysis, changes in the quality, volume, and thickness of hair.\n2. To gauge patient satisfaction with hair changes and application process.\n3. Monitor and report any adverse events associated with the daily intake of Xtressé\n\nParticipants who qualify will complete 3 visits after voluntary consent has been given. Participants will be given a 90-day supply of the gummies at visits 1 and 2 to cover the 6-month study period. Photographs and scalp analysis will be performed at each visit to measure changes in hair volume, thickness, and growth.",[27,28,29],"Androgenic Alopecia","Hair Loss\u002FBaldness","Hair Thinning","NOT_YET_RECRUITING","2026-06-08",{"date":33,"type":34},"2026-06-10","ACTUAL",{"date":36,"type":21},"2026-06-22",{"date":38,"type":21},"2027-03",{"name":40,"class":41},"Restore Biologics Holdings, Inc. dba Xtressé","INDUSTRY",2,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":50,"sex":51,"minAge":52,"maxAge":18,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":71,"locationsCount":42},"100596133","evaluating-the-combined-use-of-supplement-and-serum-in-promoting-hair-growth-in-women-with-self-perceived-thinning-hair-100596133","NCT07041489","Evaluating the Combined Use of Supplement and Serum in Promoting Hair Growth in Women With Self-perceived Thinning Hair","A Multi Center, Randomized, Double-Blind, Placebo-controlled Trial With Extension to an Open-Label Study to Evaluate the Safety and Efficacy of Xtressé™ Supplement + Serum Treatment Combination in Promoting Hair Growth in Women With Self-perceived Thinning Hair","Inclusion Criteria:\n\n* Female adults between 28-65 years of age with consistent self-perceived thinning hair.\n* Ludwig Scale I or II (mild to moderate thinning hair loss), assessed clinically.\n* Fitzpatrick Skin Types I to VI.\n* Agree to maintain their current diet, medications, exercise routines, hair shampooing, and color treatment frequency for the duration of the study.\n* Ability and willingness to comply with the study protocol including regular visits and product application.\n* Written informed consent obtained, including written consent to allow photographs to be used as part of the study data and documentation.\n* For females of childbearing potential, a negative pregnancy test at screening and commitment to effective contraception throughout the study (oral \u002F implant\u002F injectable\u002F transdermal contraceptives, intrauterine device, condom, diaphragm, abstinence, or a monogamous relationship with a partner who has had a vasectomy) to avoid pregnancy-related hormonal changes affecting hair density.\n\nExclusion Criteria:\n\n* Pregnant or lactating or planning to become pregnant.\n* Changes in hormonal therapy within 6 months prior to enrollment and throughout the study.\n* Use of other medical hair loss treatments (e.g., Minoxidil, Dutasteride, Finasteride, laser or light therapy) within 3 months prior to study start and throughout the study.\n* Micro-needling, PRP, or any other physical treatment modality on the scalp (within 6 months prior to study start and throughout the study).\n* Use of GLP-1 inhibitors (e.g., Semaglutide) within 6 months prior to study start and throughout the study.\n* Known uncontrolled health conditions (e.g., thyroid disease, anemia) that could confound study outcomes.\n* Known sensitivity to any of the ingredients in the study medication.\n* In the investigator's opinion, evidence of unwillingness, or inability to follow the restrictions and requirements of the protocol and complete the study.\n* Subject has any conditions, findings in history, physical exam or laboratory assessments, which in the opinion of the investigator, would exclude the subject from continuing in this study.\n* Treatment with an experimental drug, biologic or device within 12 weeks of the screening visit.",true,"FEMALE","28 Years",{"count":54,"type":21},85,[24],"The goal of this clinical trial is to test how safe and effective it is to improve hair growth using an active gummy and serum combination treatment when compared to an inactive treatment combination in women with self-perceived thinning hair.\n\nThe main questions this trial aims to answer are:\n\n* to confirm using photograph analytics, how much hair growth has increased in a marked area when using active treatment versus inactive treatment, and\n* participants assessment and satisfaction with the hair growth using scaled assessments.\n\nParticipants who qualify will be asked to complete 6 to 7 visits after voluntarily consent has been given. The study is divided into two parts. In Part A participants will be randomly given either active or inactive treatment to use over 3 months. After 3 months, all participants will enter Part B of the study and will be given active treatment to use over the final 6 months of the study.",[29],[59,60,61,62],"hair thinning","thinning hair","hair loss","thin hair","RECRUITING","2025-06-18",{"date":66,"type":34},"2025-06-27",{"date":68,"type":34},"2025-05-20",{"date":70,"type":21},"2026-03-30",{"name":72,"class":73},"The Center for Clinical and Cosmetic Research","OTHER",{"id":75,"slug":76,"hasResults":11,"nctId":77,"briefTitle":78,"officialTitle":78,"acronym":4,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":80,"minAge":81,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":22,"phases":84,"briefSummary":87,"conditions":88,"keywords":95,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":42},"100582895","phase-1-autologous-adipose-cells-therapy-100582895","NCT06869252","Autologous Adipose Cells Therapy","Inclusion Criteria:\n\n1. Outpatients who express interest in skin rejuvenation, and\u002For who are experiencing skin conditions, such as winkles, fine lines, loss of skin elasticity, skin pigmentation, scarring.\n2. Outpatients who are experiencing hair loss or hair thinning\n3. Provision of signed and dated informed consent form\n4. Clearly stated willingness to comply with all the procedures of the study and availability of the study\n5. Female and Male aged between 21 to 80 years old 6 Medical clearance by family doctor\n\nExclusion Criteria:\n\n1. Pregnancy or lactation\n2. Known allergic reaction to components of cell culture media\n3. Chronic disease , e.g. cardiovascular disease, diabetes, chronic kidney disease, seizures\n4. Chronic infections, e.g. skin fungi infection, psoriasis\n5. Chronic wound healing\n6. Currently taking hormone therapy\n7. History of cancers and active cancers\n8. Viral infection, e.g. HIV, hepatitis B, influenza, coronaviruses.","ALL","21 Years","80 Years",{"count":20,"type":21},[85,86],"PHASE1","PHASE2","Autologous Adipose Cell Therapy is a series of process designated to address the demerits of the traditional autologous fat grafting and dermal fillers, while enhancing the versatility and aesthetic outcomes. In this study, the goal is to evaluate the safety and efficacy of Autologous Adipose cell Therapy for skin rejuvenation and hair improvement in human application.",[28,89,90,91,92,29,93,94],"Wrinkle Appearance","Volume","Fine Lines","Skin Elasticity","Skin Pigmentation","Skin Texture",[96,97],"Adipose Cells","Adipocytes","2025-05-30",{"date":100,"type":34},"2025-05-31",{"date":102,"type":21},"2025-08-01",{"date":104,"type":21},"2026-02-01",{"name":106,"class":41},"CERM INC.",{"id":108,"slug":109,"hasResults":11,"nctId":110,"briefTitle":111,"officialTitle":112,"acronym":113,"eligibilityCriteria":114,"healthyVolunteers":50,"sex":51,"minAge":115,"maxAge":116,"enrollmentInfo":117,"targetDuration":4,"studyType":22,"phases":119,"briefSummary":120,"conditions":121,"keywords":124,"overallStatus":63,"whyStopped":4,"lastUpdateSubmitDate":128,"lastUpdatePostDateStruct":129,"startDateStruct":131,"completionDateStruct":133,"leadSponsor":135,"locationsCount":137},"100562440","benefit-of-bovine-or-marine-collagen-vs-placebo-on-skin-hair-nails-and-whole-body-health-in-healthy-adults-100562440","NCT06603194","Benefit of Bovine or Marine Collagen Vs. Placebo on Skin, Hair, Nails and Whole Body Health in Healthy Adults","BECOME Study: Comparative Efficacy of Bovine and Marine Collagen Versus Placebo on Skin, Hair, Nails and Whole Body Health Markers","BECOME","Inclusion Criteria:\n\nFemales aged 35-55 years. Participants must be comfortable with bovine or marine collagen (non-vegan\u002Fvegetarian).\n\nMust provide informed consent and be willing to comply with study requirements.\n\nExclusion Criteria:\n\nPregnant or breastfeeding women. History of chronic skin conditions (e.g., eczema, psoriasis) that might interfere with study outcomes.\n\nAny active skin infections or severe acne. Currently taking collagen supplements or have taken them within the last 6 months.\n\nUse of medications or topical agents that can affect skin, hair, nails, or gastrointestinal health (e.g., corticosteroids, retinoids).\n\nExcessive alcohol consumption or current smokers. Regular use of sunbeds. Recent cosmetic procedures (e.g., Botox, fillers, chemical peels, laser treatments) on skin, hair, or nails within the last 3 months.\n\nAny condition or situation that, in the opinion of the investigator, may interfere with the participant's ability to comply with the study requirements or give informed consent.\n\nPoor adherence to previous study protocols","35 Years","55 Years",{"count":118,"type":21},90,[24],"The BECOME Study (Bovine and Marine Collagen Efficacy for Skin, Hair, Nails and Whole Body Health Markers Evaluation) is a randomized controlled trial designed to compare the effects of bovine and marine collagen supplements versus a placebo on skin, hair, nails and whole body health markers. The trial aims to determine the most efficacious collagen source for improving health outcomes and to establish if both types of collagen are equally effective. Participants will be assessed on various health parameters, including skin elasticity, joint health, digestive health, and overall well-being, over a specified period.",[122,29,123],"Skin Laxity","Nails",[125,126,127],"Collagen","Skin health","Skin density","2024-09-16",{"date":130,"type":34},"2024-09-19",{"date":132,"type":34},"2024-08-26",{"date":134,"type":21},"2024-12-20",{"name":136,"class":41},"Ancient + Brave",1]