[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"digestive-comfort\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:digestive-comfort":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"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":45},"100651857","a-clinical-trial-to-evaluate-the-effects-of-a-powder-supplement-in-supporting-lean-muscle-development-hormone-related-wellness-digestive-comfort-dermatologic-health-and-overall-wellness-100651857",false,"NCT07766395","A Clinical Trial to Evaluate the Effects of a Powder Supplement in Supporting Lean Muscle Development, Hormone-Related Wellness, Digestive Comfort, Dermatologic Health, and Overall Wellness","Inclusion Criteria:\n\n* Be female.\n* Be aged 21-45.\n* Engages in structured physical activity ≥3 times per week, with each session lasting at least 30 minutes, (e.g., running, gym\u002Fstrength training, cycling, team sports, fitness classes).\n* Anyone with a menstrual cycle between 24-38 days.\n* Anyone who has experienced concerns with at least two of the following, twice per week, over the past four weeks: Hair, skin, and nail health\n* Bloating\n* Symptoms of hormonal imbalance.\n* Anyone with a BMI of 18.5 to 30 kg\u002Fm2.\n* Anyone who is generally healthy - does not live with any uncontrolled chronic disease.\n* If taking medications, other supplements, or herbal remedies targeted at lean muscle development, muscular endurance, digestive comfort, hormonal balance, or dermatological health, has been consistently taking for at least three months prior to starting the study, and is willing to maintain this routine for the study duration.\n* Anyone who is willing to maintain their current diet, sleep pattern, and activity levels for the duration of the trial.\n* Resides in the United States.\n\nExclusion Criteria:\n\n* Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and mental health disorders.\n* Anyone with a known history of severe digestive disorders like acid reflux, Irritable Bowel Syndrome (IBS), Irritable Bowel Disease (IBD), Crohn's disease, or gastrointestinal tract surgeries.\n* Planning on introducing any products or any new forms of prescription medication or supplements that target lean muscle development, muscular endurance, digestive comfort, hormonal balance, or dermatological health for the study duration.\n* Anyone who has been diagnosed with kidney disease and\u002For has previously or is currently taking diuretics or kidney medications.\n* Anyone who has previously or is currently taking any hormone therapies.\n* Anyone who is currently taking medications or supplements that contain zinc or iron.\n* Anyone with any allergies or sensitivities to fish, eggs, or any of the study product ingredients.\n* Anyone currently consuming products with creatine.\n* Anyone diagnosed with a thyroid-related condition.\n* Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period).\n* Anyone who has a history of serious illness in the last three months.\n* Anyone who has planned surgery during the study period.\n* Anyone with a history of substance abuse.\n* Anyone who is currently a smoker or has been a smoker in the past 3 months.\n* Anyone who has stopped or started using hormonal birth control in the past 2 months.\n* Anyone who is vegan and\u002For does not consume animal products for any reason.\n* Anyone currently taking a weight loss medication, including but not limited to Wegovy, Mounjaro, and Ozempic.\n* Currently undergoing hair treatment or using other hair growth\u002Fthickening products.\n* Currently taking any prescription medication for hair loss.\n* Anyone with any conditions that affect the hair or scalp (e.g., alopecia areata).\n* Anyone who drinks heavily (8 or more alcoholic drinks per week).",true,"ALL","21 Years","45 Years",{"count":20,"type":21},35,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study will evaluate the effects of Clean Nutra's Shelf Builder Women's Creatine Powder on lean muscle development, hormone-related wellness, digestive comfort, dermatological health, and overall wellness. The study is a single-arm, open-label, virtual trial in which all 35 enrolled participants will use the test product once daily for eight weeks.\n\nParticipants will complete self-reported questionnaires at Baseline and at the end of Week 4 and Week 8 to assess changes in lean muscle development, muscular endurance, hormone-related wellness, digestive comfort, hair\u002Fnail\u002Fskin health, and overall wellness.",[27,28,29,30,31,32],"Lean Muscle Development","Muscular Endurance","Hormone-Related Wellness","Digestive Comfort","Dermatologic Health","Overall Wellness","RECRUITING","2026-08-11",{"date":36,"type":37},"2026-08-14","ACTUAL",{"date":39,"type":21},"2026-09",{"date":41,"type":21},"2026-11",{"name":43,"class":44},"Clean Nutraceuticals","INDUSTRY",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":15,"sex":16,"minAge":52,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":4,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":4},"100648412","a-clinical-trial-to-evaluate-the-effects-of-the-edgeease-pmam-system-on-mood-mental-clarity-sleep-quality-and-digestive-wellbeing-100648412","NCT07721506","A Clinical Trial to Evaluate the Effects of the Edge+Ease PM+AM System on Mood, Mental Clarity, Sleep Quality, and Digestive Wellbeing","Inclusion Criteria:\n\n* Male and female adults aged 18 to 65 years.\n* Self-reports difficulty falling asleep, staying asleep, or having poor sleep quality overall, in the last 4 weeks.\n* Self-reports seeking support in at least one of the following domains: Difficulty switching off, perceived stress load, mental overload, next-day mental fatigue, reduced mental clarity or reduced cognitive readiness.\n* Generally healthy.\n* Willing and able to take the PM product (one serving mixed in water) in the evening and the AM product (two capsules with food) in the morning daily for 12 weeks.\n* Willing to maintain current diet, exercise, caffeine, alcohol, and sleep routines for the duration of the study.\n* Willing to wear a Fitbit continuously during the trial, and for 7 days prior to starting the test product.\n* Resides in the United States.\n\nExclusion Criteria:\n\n* Known allergy or hypersensitivity to any ingredient in the test product.\n* Currently pregnant, breastfeeding, or trying to conceive, or will be during the study period.\n* Currently undergoing treatment for cancer, or have had a serious illness requiring hospitalization in the last 3 months.\n* Diagnosed severe psychiatric disorder (e.g., bipolar disorder, schizophrenia, major depressive disorder requiring active treatment adjustment) that, in the judgment of the Investigator, would compromise participation or interpretation of results.\n* Diagnosed inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis), celiac disease, or other significant gastrointestinal condition requiring active management.\n* Current use of prescription antidepressants\u002Fanxiolytics, or other prescription neurologically-active medications that have been initiated or had a dose change within the past 90 days.\n* Current use of prescription sleep medications.\n* Regular use (i.e. more than once per week) of melatonin, sedating antihistamines, CBD\u002FTHC used for sleep, valerian, ashwagandha, or other sleep-targeted supplements.\n* Initiation of a new dietary supplement targeted at sleep, mood, cognition, or digestion within the 30 days prior to enrollment, or planning to start such a supplement during the study.\n* Heavy drinkers, defined as more than 8 alcoholic drinks per week for women and more than 15 alcoholic drinks per week for men.\n* Currently taking thyroid medication.\n* Currently testing, or plan to in the next 12 weeks, a product for another research study.","18 Years","65 Years",{"count":20,"type":21},[24],"This is a decentralized, single-arm, open-label clinical trial evaluating the effects of the Edge+Ease PM+AM dietary supplement system on sleep quality, mood, mental clarity, focus, and digestive comfort in 35 generally healthy adults aged 18-65 years over 12 weeks of daily use.\n\nParticipants will take the Edge+Ease PM product (one serving of powder mixed in approximately 150-250 mL water) in the evening approximately 60-90 minutes before bedtime, and the Edge+Ease AM product (two capsules) in the morning with food. All study activities are conducted remotely via the Citruslabs platform. Participants will complete questionnaires at Baseline, Week 4, Week 8, and Week 12, and will wear a Fitbit continuously beginning 7 days before product use through the end of the 12-week intervention period to provide objective sleep data.",[58,59,60,61,30,62,63],"Sleep Quality","Mood","Mental Clarity","Brain Fog","Focus","Evening Wind-Down","NOT_YET_RECRUITING","2026-07-18",{"date":67,"type":37},"2026-07-23",{"date":69,"type":21},"2026-08",{"date":71,"type":21},"2026-12",{"name":73,"class":44},"Edge+Ease"]