[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"parapharyngeal-or-skull-base-lesions\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:parapharyngeal-or-skull-base-lesions":31},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"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":23,"briefSummary":25,"conditions":26,"keywords":33,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":5},"100635427","full-wrap-versus-conventional-suspension-for-reducing-soft-palate-injury-rate-100635427",false,"NCT07552545","Full-wrap Versus Conventional Suspension for Reducing Soft Palate Injury Rate","Full-wrap Versus Conventional Suspension for Reducing Soft Palate Injury Rate in Transoral Surgery: A Prospective Randomized Controlled Trial","Inclusion Criteria:\n\n* Voluntarily sign the informed consent form; for patients aged \\\u003C18 years, the informed consent form must be signed by their legal guardian.\n* Age between 2 and 70 years (inclusive), male or female.\n* Patients requiring transoral surgery of the nose, pharynx, parapharyngeal space, or skull base, in which intraoperative soft palate suspension is needed.\n* Intact soft palate mucosa with no ulcers, scars, or other lesions before surgery.\n\nExclusion Criteria:\n\n* Congenital cleft palate or submucous cleft palate.\n* Patients with limited cervical spine mobility, micrognathia, or other conditions affecting surgical exposure.\n* Pregnant or breastfeeding women.\n* Presence of markedly abnormal laboratory test results, such as significant abnormalities in routine blood tests, blood biochemistry, liver and kidney function, or coagulation function.\n* Patients with active infection or infectious diseases.\n* Severe cardiac insufficiency (NYHA class III-IV).\n* Other conditions deemed unsuitable for surgery after evaluation (e.g., concomitant severe heart, brain, or lung diseases; high anesthetic risk; patients not fit for surgery).","ALL","2 Years","70 Years",{"count":20,"type":21},138,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate whether the use of full-wrap suspension, compared with the traditional double-strap suspension, can effectively reduce the risk of intraoperative and postoperative soft palate injury in transoral\u002Ftransnasal pharyngeal surgery. Through a prospective, multicenter, randomized controlled design, this study will provide evidence-based support for the clinical promotion and standardized application of full-wrap suspension.",[27,28,29,30,31,32],"Adenoid Hypertrophy","Tonsillar Hypertrophy","Nasopharyngeal Diseases","Nasopharyngeal Tumors","Parapharyngeal or Skull Base Lesions","Required Soft Palate Suspension",[34,35,36,37,38],"soft plate injury","Transoral pharyngeal surgery","Soft palate suspension","Randomized controlled trial","Full-wrap suspension","NOT_YET_RECRUITING","2026-05-05",{"date":42,"type":43},"2026-05-08","ACTUAL",{"date":45,"type":21},"2026-04-30",{"date":47,"type":21},"2027-10-31",{"name":49,"class":50},"Sun Yat-sen University","OTHER"]