[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hair-health\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hair-health":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100650168","a-clinical-trial-to-evaluate-the-effects-of-nailas-collagen-marine-plus-food-supplement-on-skin-hydration-elasticity-fine-lines-and-wrinkles-and-hair-and-nail-health-100650168",false,"NCT07746076","A Clinical Trial to Evaluate the Effects of Naila's Collagen Marine Plus Food Supplement on Skin Hydration, Elasticity, Fine Lines and Wrinkles, and Hair and Nail Health","Inclusion Criteria:\n\n* Healthy adults aged 40-60 years at the time of enrollment.\n* Self-reported visible signs of skin aging, including at least one of the following: fine lines, wrinkles, reduced skin firmness or elasticity, or skin dryness.\n* Self-reports hair shedding and a desire to improve hair health.\n* Willing to take one sachet of the study product daily for 12 weeks as directed.\n* Willing to avoid taking any other collagen-containing dietary supplements for the duration of the study.\n* Willing to maintain current diet, skincare routine, sleep patterns, and physical activity levels for the duration of the trial.\n* Willing and able to submit standardized facial and hair photographs at Baseline and Week 12.\n* Has access to a smartphone or digital camera capable of producing photographs.\n* Resides in the United States.\n* Willing to follow the study protocol and complete all required questionnaires.\n\nExclusion Criteria:\n\n* Known allergy or sensitivity to fish, marine-derived products, or any of the study product ingredients (marine collagen, hyaluronic acid, ascorbic acid, biotin).\n* Previous diagnosis of a hair loss condition such as alopecia areata, androgenetic alopecia, or telogen effluvium.\n* Currently taking any collagen-containing dietary supplements, or planning to start taking any collagen supplements in the next 12 weeks.\n* Any current uncontrolled chronic medical condition that would prevent the participant from safely completing the study protocol.\n* History of a diagnosed dermatological condition that significantly affects facial skin appearance (e.g., severe eczema, psoriasis, rosacea, or active acne) and could confound assessment of skin aging outcomes.\n* Use of prescription retinoids, injectable dermal fillers, botulinum toxin, chemical peels, laser skin treatments, or other professional aesthetic procedures on the face within 3 months prior to enrollment or planned during the study period.\n* Currently pregnant, breastfeeding, or planning to become pregnant during the study period.\n* Currently participating in another research study or planning to participate in another study during this study's duration.\n* Any condition that, in the judgment of the investigator, would make the participant unsuitable for inclusion in the study.",true,"ALL","30 Years","60 Years",{"count":20,"type":21},40,"ESTIMATED","INTERVENTIONAL",[24],"NA","This is a single-group, open-label, virtual (decentralized) clinical trial evaluating the effects of Naila's Collagen Marine Plus Food Supplement on skin hydration, elasticity, firmness, fine lines and wrinkles, and hair and nail health over 12 weeks. Forty healthy adults aged 40-60 years with self-reported mature skin showing early signs of aging will take one sachet of the supplement daily and complete questionnaires at Baseline, Week 4, Week 8, and Week 12.\n\nParticipants will also submit standardized facial and hair photographs at Baseline and Week 12 for evaluation by a board-certified dermatologist. The primary objectives are to assess changes in skin aging parameters and hair health. Secondary objectives include evaluation of nail health, hair shedding and density, participant-reported satisfaction, and product safety and tolerability.",[27,28,29,30,31,32],"Skin Aging","Skin Hydration","Skin Elasticity","Fine Lines and Wrinkles","Hair Health","Nail Health","NOT_YET_RECRUITING","2026-08-03",{"date":36,"type":37},"2026-08-04","ACTUAL",{"date":39,"type":21},"2026-08",{"date":41,"type":21},"2026-11",{"name":43,"class":44},"Gulf Bird","INDUSTRY",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":15,"sex":16,"minAge":52,"maxAge":18,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":70},"100609523","effects-of-ksm-66-ashwagandha-300-mg-on-skin-and-hair-health-in-healthy-men-and-women-100609523","NCT07215689","Effects of KSM-66 Ashwagandha® (300 mg) on Skin and Hair Health in Healthy Men and Women\"","A Prospective, Randomized, Double-Blind, Placebo Controlled Clinical Study to Evaluate the Effects of KSM- 66 Ashwagandha® Capsule (300 mg) on Skin and Hair Health in Healthy Men and Women","Inclusion Criteria:\n\n1. Healthy adult men and women participants ≥ 18 years and ≤60 years of age.\n2. Willingness to follow the protocol requirements as evidenced by written informed consent.\n3. Participants who were on consistent dietary, hair, and skin product 3 months prior to start of the study and are willing to follow the same during the study.\n4. Participants who agree not to use any medication (prescription and over the counter), including vitamins and minerals, during or before the course of this study.\n5. Participants with mild to moderate hair loss classified as the Norwood-Hamilton type II, III, IV and V in males and Ludwig type I and II in females.\n6. Willing to come for all follow-up visits.\n7. Participants who agree not to cut hair for the entire duration of the study.\n8. Participants willing to undergo Trichoscan evaluation and not to wash their hair 48 hours before the visit.\n9. Participants or LAR can and willing to give meaningful, written informed consent prior to participation in the trial, in accordance with regulatory requirements.\n10. Participants who agree to take investigational product (i.e., Till Day 90 ± 4 ± 4).\n\nExclusion Criteria:\n\n1. Participants having any clinically significant medical history, medical finding including rosacea, eczema, psoriasis, and atopic dermatitis or an on-going medical or psychiatric condition exists which in the opinion of the Investigator could jeopardize the safety of the subject, impact validity of the study results or interfere with the completion of study according to the protocol.\n2. Participants on any medication or supplement for hair loss, including finasteride, any other 5 α-reductase inhibitor, minoxidil, steroids, or hormonal products, during the 3 months prior to study commencement.\n3. Participants having a history of hypersensitivity reactions (i.e., allergic or oversensitivity to study medication).\n4. Participants who have undergone or plan to undergo hair transplantation surgery during the study period.\n5. Participants with facial skin cancer.\n6. Participants with sunburn, moderate to pronounced suntan, uneven skin tones, tattoos, scars or other disfiguration, dilated vessels or other conditions on the test area that might influence the test results.\n7. Participants with severe seborrheic dermatitis, alopecic disease, except for androgenic alopecia, and scalp disorders, such as scalp psoriasis and infection.\n8. Participants who have participated in a clinical study during the preceding 180 days.\n9. Participants having eating disorders (i.e., bulimia, psychogenic eating disorders, etc.).\n10. Pregnant and lactating females\n11. Participants with alcohol addiction or persistent abuse of drugs of dependence.","18 Years",{"count":54,"type":21},50,[24],"Hair and skin play major roles in protecting the body, and maintaining their health is essential. Poor hair and skin health have become increasingly common due to the stress associated with modern lifestyles. Effective and time-efficient treatments for hair and skin health remain limited. Although hair loss, baldness, and skin issues are not life-threatening, managing these conditions is important because of the psychological and social complications-such as anxiety and depression-they can cause. There is an unmet need for therapies that provide safe and long-term improvements in hair and skin health.\n\nMany individuals seek Complementary and Alternative Medicine (CAM) to identify natural and effective options for these conditions. Adaptogens such as Ashwagandha (Withania somnifera) have long been studied for their potential to reduce stress and modulate cortisol levels in the body. Reducing stress may help prevent inflammation, a common contributor to hair shedding and loss. Ashwagandha also contains antioxidants and amino acids that may strengthen the hair and minimize breakage. Traditionally, Ashwagandha has been recognized for its multiple health benefits, including support for hair and skin wellness. However, there remains limited scientific evidence to substantiate these traditional claims, underscoring the need for controlled clinical evaluation.",[58,31],"Skin Health","RECRUITING","2025-10-10",{"date":62,"type":37},"2025-10-15",{"date":64,"type":37},"2025-07-11",{"date":66,"type":21},"2025-12-10",{"name":68,"class":69},"SF Research Institute, Inc.","NETWORK",1]