[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vascular-lesion\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vascular-lesion":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,70],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":20,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":27,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100593917","outcomes-and-risk-factors-of-different-treatment-strategies-for-neuro-co-cardiological-diseases-and-post-cardiac-surgery-cerebrovascular-diseases-100593917",false,"NCT07012668","Outcomes and Risk Factors of Different Treatment Strategies for Neuro-co-cardiological Diseases and Post-cardiac Surgery Cerebrovascular Diseases","Inclusion Criteria:\n\n1. Age ≥18 years;\n2. Patients with neuro-co-cardiological diseases or post-cardiac surgery cerebrovascular diseases.\n\nExclusion Criteria:\n\n1. The expected survival is less than 1 years;\n2. Simultaneously merge other serious diseases;","ALL","18 Years",{"count":18,"type":19},2000,"ESTIMATED","1 Year","OBSERVATIONAL","The objective of this observational cohort study is to evaluate the clinical outcomes of various treatment strategies for cerebrovascular and cardiovascular diseases. Furthermore, it aims to investigate the factors that influence adverse outcomes from these treatments.",[24,25,26],"Neuro-co-cardiological Diseases","Post-cardiac Surgery Cerebrovascular Diseases","Vascular Lesion",[28,29,30,31,32],"Neuro-co-cardiological diseases","Post-cardiac surgery Cerebrovascular diseases","Simultaneous treatment","Staged treatment","Conservative treatment","RECRUITING","2025-06-09",{"date":36,"type":37},"2025-06-12","ACTUAL",{"date":39,"type":37},"2024-09-19",{"date":41,"type":19},"2027-09-19",{"name":43,"class":44},"Beijing Anzhen Hospital","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":15,"minAge":16,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":45},"100533816","oxygenation-in-vascular-lesions-of-the-colon-100533816","NCT06230731","Oxygenation in Vascular Lesions of the Colon","Inclusion Criteria:\n\n* Undergo standard of care colonoscopy\n* People with a history of vascular lesions of the colon\n* People with healthy colon\n* 18 - 89 years of age\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years\n* Age \\> 90 years\n* People with ulcerations in at ascending colon opposite the ileocecal valve\n* Previous colon surgery",true,"89 Years",{"count":55,"type":19},30,"INTERVENTIONAL",[58],"NA","The goal of this clinical trial is to evaluate oxygenation in the colon in people with acquired vascular abnormalities in the proximal colon.",[26],"2025-06-05",{"date":63,"type":37},"2025-06-10",{"date":65,"type":37},"2024-02-01",{"date":67,"type":19},"2029-02-01",{"name":69,"class":44},"University of Chicago",{"id":71,"slug":72,"hasResults":11,"nctId":73,"briefTitle":74,"officialTitle":75,"acronym":76,"eligibilityCriteria":77,"healthyVolunteers":52,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":78,"targetDuration":4,"studyType":56,"phases":80,"briefSummary":81,"conditions":82,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":86,"lastUpdatePostDateStruct":87,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":96},"100566434","intense-pulsed-light-ipl-medical-device-as-treatment-for-patient-suffering-from-skin-disorder-100566434","NCT06655129","Intense Pulsed Light (IPL) Medical Device as Treatment for Patient Suffering From Skin Disorder","Post Market Clinical Study of an Intense Pulsed Light (IPL) Medical Device as Treatment for Patient Suffering From Skin Disorder","Anthelia","Inclusion Criteria:\n\n* Adult men or women\n* Excessive Hairiness:\n* Patient with unwanted hair on the body (legs, arms, bikini line, or axilla)\n* Patient over 18 years.\n* Patients with Fitzpatrick skin types from I to V.\n* Women were required to be post-menopausal, surgically sterilized, or under a medically acceptable form of birth control (i.e., oral contraceptives, IUD, contraceptive implant, or barrier methods with spermicide or abstinence) during the study time period.\n\nVascular lesions:\n\n* Patients over 18 years.\n* Patients with Fitzpatrick skin types from I to IV.\n* Patients with varicosities and Rosacea on the face or upper and lower limbs.\n\nPigmented lesions:\n\n* Patients over 18 years.\n* Patients with solar lentigines on their cheeks, back, hands, arm and leg (\\> 3 mm).\n* Patient with Fitzpatrick skin type from I to IV.\n\nAcne:\n\n* Patients over 18 years\n* Patients with Fitzpatrick skin types from I to IV.\n* Patients with facial acne vulgaris on face.\n* Willing to sun protect treated area for the duration of enrollment in the study and 4 weeks after treatment.\n\nExclusion Criteria:\n\n* Patients with history of malignant lesions or pre-malignant lesions, scarring, or infection in the area to be treated History of keloidal or hypertrophic scarring\n* Patients with a known photosensitivity\n* Pregnancy women\n* Patient with diabetes mellitus suntan in the area to be treated\n* Use of photo-sensitizing products for 7 days before treatment (selftanning lotions, activators, self-tanning shower gel, etc.)\n* Exposure to the sun or UV rays at least 4 weeks before the treatment and 1 week afterwards\n* Zones with uncovered tattoos, suspect spots or skin diseases (including spots, inflammation, beauty spots, tumors or melanomas, psoriasis, herpes...)\n* Use of medication that induces anticoagulative medication or thromboembolic condition\n* Patients with pacemaker or internal defibrillator\n* Patients that used of NSAIDS two weeks prior to or 2 weeks following the treatment\n* Epileptic patients\n* Additional criteria for excessive hair: Patients that use waxing or other methods of photo epilation within 1 month prior to treatment.\n* Additional criteria for acne: Patients currently under oral antibiotic or oral therapy for acne.",{"count":79,"type":19},85,[58],"The first IPL device obtained United States Food and Drug Administration (FDA) clearance in 1995 for treatment of lower extremity telangiectasias. Since then, its favorable cost and versatility in contrast to many singlespectrum lasers, has led to its rapid proliferation and use in a number of different clinical settings. As described in the literature, ANTHÉLIA medical device is intended to treat skin disorders:\n\n* Excessive Hairiness (Hirsutism, Hypertrichosis...)\n* Vascular lesions (Rosacea….)\n* Pigmented lesions (Lentigo et melasma)\n* Acne vulgaris",[83,26,84,85],"Excessive Hairiness","Pigmented Lesions","Acne Vulgaris","2024-10-21",{"date":88,"type":37},"2024-10-23",{"date":90,"type":37},"2024-01-20",{"date":92,"type":19},"2025-12-01",{"name":94,"class":95},"Eurofeedback","INDUSTRY",5]