[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100548821":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":30,"locations":40,"responsibleParty":57,"collaborators":59,"id":63,"slug":64,"hasResults":65,"nctId":66,"briefTitle":67,"officialTitle":68,"acronym":69,"eligibilityCriteria":70,"healthyVolunteers":65,"sex":71,"minAge":72,"maxAge":73,"enrollmentInfo":74,"targetDuration":25,"studyType":77,"phases":78,"briefSummary":80,"conditions":81,"keywords":25,"overallStatus":43,"whyStopped":25,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":93},{"fullName":5,"class":6},"Fundacion Dexeus","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Cellular Matrix \u002F A-CP-HA Kit","EXPERIMENTAL","(a combination of autologous platelet-rich plasma and non-cross-linked hyaluronic acid) is a sterile tube designed for use in the preparation of a mixture of PRP and hyaluronic acid, tube is under vacuum allowing the withdrawal of 6 ml of blood and contains: 2 ml of hyaluronic acid gel (20mg\u002Fml, 40 mg per tube) in phosphate buffer. Not crosslinked, hyaluronic acid is obtained from bacterial fermentation, 3 g of inert cell-selector gel, and 0.6 ml of anticoagulant (sodium citrate 4%). Centrifuged at 1,500 g, 3,000 rpm for 5 min. Platelet recovery of more than 70%, granulocyte depletion of 94.3% and red blood cells of 99.5% are achieved.",[13],"Drug: Cellular Matrix \u002F A-CP-HA Kit",{"label":15,"type":16,"description":17,"interventionNames":18},"Local estrogen therapy","ACTIVE_COMPARATOR","Blissel, estriol 50 micrograms\u002Fg vaginal gel",[19],"Drug: Local estrogen therapy (Blissel, estriol 50 micrograms\u002Fg vaginal gel)",[21,26],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","For infiltration, a prior preparation of the region with anesthetic cream is performed, procaine 25 mg\u002Fg + lidocaine 25 mg\u002Fg (Emla 5% cream) in the vulvar area and vaginal introitus. Occlusion of the area with plastic film is performed for 20 minutes. After asepsis and antisepsis, infiltration is performed with mesotherapy needles 31G 4mm, using the technique of superficial \"point-to-point\" mesotherapy microinjections, in the vestibule and the first 3 cm of the posterior wall of the vagina.",[9],null,{"type":22,"name":27,"description":28,"armGroupLabels":29,"otherNames":25},"Local estrogen therapy (Blissel, estriol 50 micrograms\u002Fg vaginal gel)","Blissel®, Estriol vaginal gel 50 micrograms\u002Fg, daily application for 15-21 days in a row, then two times a week for 24 weeks (6 months). Application instructions will be explained to the patients. The gel should be applied in the vagina using an applicator with the marked dose, the full applicator should be inserted into the vagina and emptied, preferably at night.",[15],[31,36],{"name":32,"role":33,"phone":34,"phoneExt":25,"email":35},"Antonella de Ponte Davi, MD","CONTACT","0034932274700","ANTPON@dexeus.com",{"name":37,"role":33,"phone":34,"phoneExt":38,"email":39},"Ignacio Rodríguez, MSc","22029","nacrod@dexeus.com",[41],{"facility":42,"status":43,"city":44,"state":25,"zip":45,"country":46,"countryCode":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Departamento de Ginecología Obstetricia y Reproducción. Hospital Universitari Dexeus","RECRUITING","Barcelona","08037","Spain","ES",{"type":49,"coordinates":50},"Point",[51,52],2.15899,41.38879,{"lat":52,"lon":51},[55],{"name":56,"role":33,"phone":34,"phoneExt":38,"email":39},"Ignacio Rodríguez, BsC",{"type":58,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR",[60],{"name":61,"class":62},"Regen Lab SA","INDUSTRY","100548821","phase-4-efficacy-of-the-use-of-cellular-matrix-a-cp-ha-kit-100548821",false,"NCT06425978","Efficacy of the Use of Cellular Matrix\u002F A-CP-HA Kit","The Efficacy of the Use of Cellular Matrix \u002F A-CP-HA Kit (Combination of Autologous Platelet-rich Plasma and Non-cross-linked Hyaluronic Acid) Compared to Local Estrogen Therapy (Blissel, Estriol 50 Micrograms\u002Fg Vaginal Gel) in Women With Genitourinary Syndrome of Menopause. A Randomized Controlled Trial, With a Second Blind Observer.","CellularMatrix","Inclusion Criteria:\n\n* Women ≤70 years old\n* Women that are sexually active\n* Women who report symptoms and signs of SGM, with a vaginal health index (VHIS - Bachmann score) \\\u003C 15 points.\n* Women who understand the Spanish language\n* Willing to participate in the study and sign informed consent.\n\nExclusion Criteria:\n\n* Systemic or local hormonal treatment in the last 3 months\n* Tamoxifen or Aromatase inhibitor treatments\n* Vulvovaginal pathologies (condyloma, vaginal intraepithelial neoplasia, vaginal carcinoma, lichen sclerosus, lichen planus, history of radiation, history of cervical cancer, other gynecologic cancer, or pelvic radiation, or active genital infection (eg. g., bacterial vaginosis, genital herpes, candida) Contraindication for vaginal estrogen therapy\n* Women with thrombocytopenia or coagulation disorders, systemic infections, STDs, cancer of any type in recent treatment, connective tissue diseases.\n* Women who have had pelvic surgery within 6 months.\n* Women who are unwilling or unable to give informed consent and\u002For do not comply with the study requirements.","FEMALE","18 Years","70 Years",{"count":75,"type":76},192,"ESTIMATED","INTERVENTIONAL",[79],"PHASE4","This study is a randomized, controlled, non-inferiority trial, that will be performed on 192 women on Menopause (absence of menstruation for at least 12 months), with diagnostic of genitourinary syndrome of menopause (SGM) and a vaginal health index \\\u003C15 points, that are sexually active.\n\nPatients will be randomized 1:1, equal number assigned to each of the two treatment groups, to receive treatment with two dose of Cellular Matrix \u002F A-CP-HA Kit (a combination of autologous platelet-rich plasma and non-cross-linked hyaluronic acid) separated for a month, and control group that will receive the standard treatment for SGM, local estrogen therapy (Blissel, estriol 50 micrograms\u002Fg vaginal gel).\n\nBoth groups will be follow-up for 3 and 6 month afther treatment, a blind observer will assess the application of the validated scale (VHIS, VHI), and the investigators will do the FSD, symptom record, maturation index, follow-up photography and evaluation of adverse events and treatment compliance and adherence.",[82],"Genitourinary Syndrome of Menopause","2024-07-15",{"date":85,"type":86},"2024-07-16","ACTUAL",{"date":88,"type":86},"2024-05-30",{"date":90,"type":76},"2026-08",{"name":92,"class":6},"Fundación Santiago Dexeus Font",1]