[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"septoplasty\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:septoplasty":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,50,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":4,"briefSummary":23,"conditions":24,"keywords":28,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100589172","video-laryngeal-mask-vs-endotracheal-tube-in-septoplasty-100589172",false,"NCT06950957","Video Laryngeal Mask vs. Endotracheal Tube in Septoplasty","Comparison of Video Laryngeal Mask Airway and Endotracheal Tube Use for Airway Safety in Patients Undergoing Septoplasty","Inclusion Criteria:\n\n* ASA I-II classification patients\n* Patients aged 18-65 years undergoing elective septoplasty\n\nExclusion Criteria:\n\n* ASA III-IV classification patients\n* Patients with anticipated difficult airway\n* Patients under 18 years of age\n* History of gastroesophageal reflux disease (GERD) or hiatal hernia\n* Body mass index (BMI) \\>30\n* Pregnant patients","ALL","18 Years","65 Years",{"count":20,"type":21},64,"ESTIMATED","OBSERVATIONAL","This randomized controlled trial compares a video laryngeal mask airway (VLMA) and an endotracheal tube (ETT) in adult patients undergoing elective septoplasty. The primary objective is to see which device more effectively prevents surgical blood contamination in the glottic and subglottic regions. The study also assesses perioperative hemodynamic stability, ventilation parameters, and postoperative recovery factors such as sore throat, hoarseness, and overall patient comfort. The findings aim to help determine the optimal airway device choice for nasal surgeries.",[25,26,27],"Airway Complication of Anesthesia","Anesthesia Intubation Complication","Septoplasty",[27,29,30,31,32,33,34,35,36],"Laryngeal Mask Airway","Endotracheal Tube","Postoperative Sore Throat","Airway Leak","Otorhinolaryngology Surgery","Supraglottic Airway Devices","Aldrete Score","Postoperative Sore Throat (POST Score)","RECRUITING","2025-06-11",{"date":40,"type":41},"2025-06-12","ACTUAL",{"date":43,"type":41},"2025-05-30",{"date":45,"type":21},"2025-12-01",{"name":47,"class":48},"Samsun University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":16,"minAge":57,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":61,"phases":62,"briefSummary":64,"conditions":65,"keywords":66,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":49},"100586821","different-techniques-for-prevention-of-complications-after-septoplasty-operation-100586821","NCT06920368","Different Techniques for Prevention of Complications After Septoplasty Operation","Comparative Study Between the Efficacy of Trans-Septal Quilting Sutures, Nasal Pack and Intranasal Silicon Splint in Endoscopic Septoplasty","Inclusion Criteria:\n\n* Healthy adult patient of different ages from 16 to 60 year-old with symptomatic deviated nasal septum\n\nExclusion Criteria:\n\n* Patient with nasal polyposis or nasal tumors or patients with sinusitis not responding to medical treatment.\n* Patient with previous septal operation\n* Patient who is planned to do partial inferior turbinectomy or turbinoplasty with septoplasty\n* Patients with contraindications for general surgery","16 Years","60 Years",{"count":60,"type":21},90,"INTERVENTIONAL",[63],"NA","the aim of the study is to compare complication of trans-nasal quilting sutures, nasal pack and intra intranasal silicon splint in endoscopic septoplasty",[27],[67,68,69,70,71,72],"complication","quilting","splint","pack","septoplasty","endoscopic","2025-04-13",{"date":75,"type":41},"2025-04-16",{"date":77,"type":41},"2024-05-01",{"date":79,"type":21},"2025-05-01",{"name":81,"class":48},"Tanta University",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":61,"phases":92,"briefSummary":93,"conditions":94,"keywords":96,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":49},"100585304","effects-of-methods-on-dry-mouth-after-septoplasty-surgery-100585304","NCT06900621","Effects of Methods on Dry Mouth After Septoplasty Surgery","Effects of Two Different Methods on Early Period Dry Mouth After Septoplasty Surgery","Inclusion Criteria:\n\n* Age between 18 and 89\n* Able to communicate in Turkish\n* No obstacle to communication\n* Agreeing to participate in the study\n* Conscious and oriented as a result of the evaluation made with SPMT at 30 minutes after the surgery, with a clear airway, no nausea or vomiting\n* Using silicone nasal tampons\n\nExclusion Criteria:\n\n* Patients with a preoperative oral mucous membrane integrity assessment Oral Assessment Guide (OAG) result of over 16\n* Those taking medication that affects dry mouth\n* Those with a chronic disease that affects dry mouth\n* Those undergoing a second simultaneous surgical procedure\n* Those who develop complications during surgery and\u002For during recovery from anesthesia\n* Patients who smoke will not be included in the study.","89 Years",{"count":91,"type":21},81,[63],"It was planned to investigate the effects of two different methods on early dry mouth after septoplasty surgery. The data of this study, which is planned to be conducted experimentally, is planned to be collected at Gönen State Hospital between 2025-2026. Patients who are scheduled to undergo septoplasty surgery and present with septum deviation constitute the universe of the study. The research sample (n: 63) was determined using the Power analysis G\\*Power v3.1.9.7 program by taking the sample study as reference. However, considering the data losses (dropouts) in similar studies, when the missing data rate was taken as 20% , the sample size was determined as 81 patients. Patients who were informed about the study and volunteered to participate in the study (n: 81) and met the inclusion criteria of the study will constitute the sample group. 3 groups were determined in the study as intervention groups (group 1 and group 2) and control group (group 3). Patients who meet the preoperative criteria will be randomized into one of three groups after surgery. Data will be collected using the Patient Identification Form, General Patient Follow-up Form, Nasal Obstruction Symptom Assessment Scale (NOSE), Visual Analog Scale (VAS) scoring expressed by the patient to measure mouth dryness and satisfaction, \"Safety Protocol for Thirst Management in the Immediate Postoperative Period\" (SPTM), Oral Mucous Membrane Integrity Assessment and Follow-up Form - Oral Assessment Guide (OAG). 3 groups will be created in the study. 5 ml of ice water will be applied to one group that will receive intervention, the other group will be given water at normal room temperature, and the control group will receive standard clinical care and will not be treated. As a result of the evaluation made with SPTM in the first 30 minutes after the surgery, the dry mouth of all patients included in the study (Group 1, Group 2, Group 3) who meet the conditions will be evaluated before the application, starting from the first 30 minutes after the surgery and at 60 - 90 - 120 - 150 - 180 minutes. In the study, all patients (Group 1, Group 2, Group 3) will be evaluated for dry mouth before the application. The data obtained as a result of the study will be analyzed with a statistical package program. In the evaluation of the data in the study, descriptive statistics and parametric or non-parametric tests will be applied depending on whether the data show a normal distribution. In comparisons, p\\\u003C0.05 value will be considered statistically significant.",[27,95],"Dry Mouth",[97,98,99,71,100,101],"dry mouth","nursing","early period","water at room temperature","ice water","NOT_YET_RECRUITING","2025-03-29",{"date":105,"type":41},"2025-04-03",{"date":107,"type":21},"2025-03-25",{"date":109,"type":21},"2027-12-31",{"name":111,"class":48},"Ege University"]