[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hypertrophic-scarring\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hypertrophic-scarring":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100609358","phase-4-remimazolam-vs-propofol-in-laser-burn-cases-100609358",false,"NCT07213544","Remimazolam vs Propofol in Laser Burn Cases","Comparison of Remimazolam Versus Propofol for Monitored Anesthetic Care in Elective Fractional Ablative CO₂ Laser","Inclusion Criteria:\n\n* Age ≥ 18 years\n* Undergoing both outpatient Session #1 and Session #2 of fractional ablative CO2 laser therapy\n\nExclusion Criteria:\n\n* History of previous fractional ablative laser therapy for burn scar\n* Procedure expected to last longer than 30 minutes\n* Allergy such as dextran 40 or contraindication to either of the study drugs\n* Pregnant and\u002For breastfeeding\n* Subjects who are unable to or choose not to give informed consent","ALL","18 Years",{"count":19,"type":20},136,"ESTIMATED","INTERVENTIONAL",[23],"PHASE4","This randomized, single-blind, crossover study compares remimazolam and propofol for monitored anesthetic care during fractional ablative CO₂ laser therapy for burn scars. The primary aim is to assess incidence of respiratory depression, defined as a need for advanced airway maneuvers (jaw thrust\u002Fchin lift, insertion of oral or nasal airway, or bag mask ventilation), and hypopnea (respiratory rate \\\u003C 8).",[26,27,28],"Burn Scar","Hypertrophic Scarring","Procedural Sedation","RECRUITING","2025-11-17",{"date":32,"type":33},"2025-11-20","ACTUAL",{"date":35,"type":33},"2025-11-12",{"date":37,"type":20},"2027-01-01",{"name":39,"class":40},"Medical University of South Carolina","OTHER",1,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":48,"sex":16,"minAge":17,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":41},"100524117","comparison-of-the-effects-of-liquid-vaseline-and-olive-oil-on-itching-and-scarring-in-scald-burns-100524117","NCT06104540","Comparison of the Effects of Liquid Vaseline and Olive Oil on Itching and Scarring in Scald Burns","Inclusion Criteria:\n\n* Between the ages of 18-65,\n* With a total body burn area of less than 15% 2nd degree scald burn,\n* Wwhose treatment has been completed and who do not need dressing and do not have open wounds,\n* Who do not have any allergies,\n* Who can read and write,\n* Who do not have cognitive problems,\n* Who do not have communication problems,\n* Who live in Ankara and who volunteer to participate in the study.\n\nExclusion Criteria:\n\n* Patients with burns on the face and neck,\n* Ppatients with dermatologic diseases and patients using antihistamines will not be included.\n* Patients who do not want to continue the study,\n* Who develop an allergic reaction during the follow-up period,\n* Who start treatment during the follow-up period due to itching,\n* Wwho have not applied more than 20% liquid vaseline\u002Folive oil during the 3-month follow-up period (60 applications\u002F30 days; more than 36 applications out of 180 applications) will be excluded from the study.",true,"65 Years",{"count":51,"type":20},24,[53],"NA","Pain, itching, hypertrophic scar formation after wound healing in burn patients complications, sleep disturbances in patients, anxiety, depression, and daily life It may disrupt activities and deterioration in quality of life. Liquid petroleum jelly and olive oil have no side effects, moisturizing properties, or wound-healing treatment of burns due to their positive effects on symptoms such as itching. can be used to alleviate burns. The project found the use of liquid petroleum jelly and olive oil to determine the effect on itching and scarring in burn patients. After burns reduction of symptoms such as itching, dryness, hypertrophic scarring, and patient comfort. Provision of care is a part of nursing care. In studies, itching and scarring there is insufficient evidence regarding the treatment methods applied for its treatment is observed. In addition, the effect of olive oil and liquid petroleum jelly on itching and scarring no scientific study was found. The results of the project were found to be significant in terms of post-burn itching providing evidence of hypertrophic scar management and contributing to ongoing studies is expected to be found. Since there are no similar studies in the literature, a preliminary study with 24 patient applications will be made. In line with the data obtained from the pre-application, the sample calculation will be made and the application will continue by making the necessary arrangements. Patients will be divided into experimental and control groups by simple randomization. All patient groups individual data collection forms on the first day; 12 individual data collection forms on the first day, 15th day, first, second, and third months Itemized Itch Severity Scale, Patient and Observer Scar Scale to be applied in Burn Patients and the wound area will be photographed. Patients in the control group will be given no application will be made. Liquid petroleum jelly and olive oil group before the study training will be given and they will massage the recommended product twice a day for 3 months and will be asked to record them. The data obtained at the end of the project will be statistically analyzed and results will be presented.",[56,57,27],"Scald Burn","Itching",[59,60,61,62,63,64],"scald burns","nursing care","oliveoil","liquid vaseline","itching","hypertrophic scarring","2024-07-31",{"date":67,"type":33},"2024-08-02",{"date":69,"type":20},"2024-09-01",{"date":71,"type":20},"2025-01-31",{"name":73,"class":40},"Ankara Yildirim Beyazıt University"]