[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"voice-quality\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:voice-quality":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,78],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":31,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100570879","addiction-of-lung-volume-recruitment-technique-in-lee-silverman-protocol-for-voice-professionals-100570879",false,"NCT06712979","Addiction of Lung Volume Recruitment Technique in Lee Silverman Protocol for Voice Professionals","Comparison Between Lee- Silverman Method and Lung Volume Recruitment Tecnhique in Voice Professionals","LVRTVOICE","Inclusion Criteria:\n\n* Voice professionals with no voice disease\n\nExclusion Criteria:\n\n* smokers\n* Glottis paralysis and dysfunction\n* dental problems\n* Mental and cognitive disorders",true,"ALL","20 Years","60 Years",{"count":22,"type":23},20,"ESTIMATED","INTERVENTIONAL",[26],"NA","The goal of this clinical trial in voice professionals with both genders aimed to verify the changes in the vocal range profile and the changes in the glottic and vocal tract configuration for more efficient phonation after applying the adapted Lee Silverman Method and the addiction of lung volume recruitment technique in acoustic and structural analysis.",[29,30],"Voice Quality","Singing",[32,33,34],"voice training","acoustic","respiratory therapy","RECRUITING","2026-05-23",{"date":38,"type":39},"2026-05-28","ACTUAL",{"date":36,"type":39},{"date":42,"type":23},"2026-07-31",{"name":44,"class":45},"Escola Superior de Ciencias da Saude","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":18,"minAge":55,"maxAge":4,"enrollmentInfo":56,"targetDuration":58,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":4},"100617607","quality-of-life-and-functional-outcomes-in-laryngeal-cancer-patients-100617607","NCT07320820","Quality of Life and Functional Outcomes in Laryngeal Cancer Patients","Assessment of Quality of Life, Patient Satisfaction, Swallowing Function, Voice Outcomes, Pain, and Anxiety-Depression at Baseline and at 3-, 6-, and 12-Month Follow-Up in Patients Diagnosed With Laryngeal Squamous Cell Carcinoma: A Prospective Questionnaire-Based Study","QoL in LSSC","Inclusion Criteria:\n\n* Age ≥ 18 years at the time of enrollment.\n* Histopathologically confirmed diagnosis of laryngeal squamous cell carcinoma.\n* Planned to undergo surgical treatment or radiotherapy\u002Fchemoradiotherapy as part of standard oncological care.\n* Willing and able to participate in the study and to provide written informed consent.\n* No history of psychiatric or neurological disorders that could impair comprehension, questionnaire completion, or study participation.\n\nExclusion Criteria:\n\n* Age \\\u003C 18 years.\n* Presence of comorbid conditions that may independently affect swallowing or voice functions.\n* Patients who withdraw consent or request to discontinue participation during or after the treatment period.\n* History of psychiatric disorders or use of psychiatric medications that may interfere with study participation or completion of patient-reported outcome measures.","18 Years",{"count":57,"type":23},120,"12 Months","OBSERVATIONAL","Laryngeal squamous cell carcinomas are head and neck malignancies that directly affect both swallowing and voice functions and are associated with a significant deterioration in patients' quality of life throughout the treatment process.\n\nThe aim of this study is to evaluate quality of life, voice and swallowing functions, pain, anxiety-depression levels, and patient satisfaction at the pre-treatment period and at the 3rd, 6th, and 12th months post-treatment in patients with laryngeal malignancies, using validated questionnaires, in order to:\n\nElucidate the course of functional recovery following treatment,\n\nIndividualize rehabilitation and follow-up strategies, and\n\nExamine the relationship between functional outcomes and oncological survival.",[62,63,64,29,65,66,67],"Laryngeal Carcinoma","Quality of Life (QOL)","Patient Satisfaction","Swallowing Function","Pain Management","Anxiety Depression","NOT_YET_RECRUITING","2026-04-21",{"date":71,"type":39},"2026-04-22",{"date":73,"type":23},"2026-04-02",{"date":75,"type":23},"2027-12-31",{"name":77,"class":45},"Saglik Bilimleri Universitesi",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":18,"minAge":55,"maxAge":85,"enrollmentInfo":86,"targetDuration":4,"studyType":24,"phases":88,"briefSummary":90,"conditions":91,"keywords":94,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":100,"lastUpdatePostDateStruct":101,"startDateStruct":103,"completionDateStruct":105,"leadSponsor":107,"locationsCount":46},"100633781","phase-4-effects-of-flurbiprofen-spray-and-ice-cream-for-pain-and-voice-outcomes-after-thyroidectomy-100633781","NCT07531147","Effects of Flurbiprofen Spray and Ice Cream for Pain and Voice Outcomes After Thyroidectomy","Comparison of the Effects of Postoperative Oral Flurbiprofen (0.25%) Spray and Ice Cream on Analgesia and Voice Quality in Patients Undergoing Thyroidectomy","Inclusion Criteria:\n\n* No history of neck surgery\n* Age between 18-85 years\n* Undergoing thyroidectomy\n* Agreeing to participate in the study\n* Operation duration between 60-120 minutes\n\nExclusion Criteria:\n\n* History of neck surgery\n* History of radiotherapy to the head and neck region\n* Pre-operative or post-operative vocal cord paralysis\n* Pre-operative phonetic disorder\n* Pre-operative laryngeal pathology\n* Being under 18 years of age\n* Refusal to participate in the study\n* Smoking\n* Flurbiprofen allergy\n* Lactose intolerance","85 Years",{"count":87,"type":23},100,[89],"PHASE4","Researchers will compare oral flurbiprofen (%0.25) spray and ice cream to a placebo (a look-alike substance that contains no drug) to see if oral flurbiprofen (%0.25) spray and ice cream works to effect post-thyroidectomy throat pain and voice quality.\n\nParticipants will:\n\n* Receive 1 puff of oral flurbiprofen (0.25%) spray or 105 ml of ice cream or 1 puff of oral spray prepared with drinking water (placebo) at 5 hours postoperatively according to randomization result\n* Undergo voice analysis using Praat voice analysis (University of Amsterdam) at 6 hours postoperatively\n* Undergo a visual analog scale for analgesia status at 6 hours postoperatively",[92,93,29],"Thyroidectomy","Sore Throat",[95,96,97,98,99],"thyroidectomy","sore throat","voice quality","flurbiprofen","ice cream","2026-04-11",{"date":102,"type":39},"2026-04-15",{"date":104,"type":23},"2026-04",{"date":106,"type":23},"2026-09",{"name":108,"class":45},"Izmir Katip Celebi University"]