[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Thammasat University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":233},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,8,0,[8,46,72,94,118,135,168,199],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":21,"conditions":22,"keywords":24,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100635141","gina-p-and-act-p-scores-for-assessing-asthma-control-100635141",false,"NCT07548827","GINA-P and ACT-P Scores for Assessing Asthma Control","Inclusion Criteria:\n\n* Asthma\n* Age 18 years or older\n\nExclusion Criteria:\n\n* Inability to perform spirometry test","ALL","18 Years",{"count":18,"type":19},144,"ESTIMATED","OBSERVATIONAL","The goal of this observational study is to determine the accuracy of GINA-P and ACT-P scores in assessing asthma control levels among adults with asthma.\n\nThe main question the study aims to answer is:\n\nHow accurate are the GINA-P and ACT-P scores in assessing asthma control levels among adults with asthma? Participants will complete a questionnaire on asthma symptoms and undergo pulmonary function testing.",[23],"Asthma",[25,26,27,28,29,30,31,32],"asthma","asthma control","pulmonary function","bronchodilator response","Asthma Control Test","Global Initiative for Asthma","ACT-P","GINA-P","NOT_YET_RECRUITING","2026-04-16",{"date":36,"type":37},"2026-04-23","ACTUAL",{"date":39,"type":19},"2026-05-01",{"date":41,"type":19},"2026-12-31",{"name":43,"class":44},"Thammasat University","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":54,"conditions":55,"keywords":58,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":65,"startDateStruct":67,"completionDateStruct":69,"leadSponsor":70,"locationsCount":71},"100618162","remission-in-adults-with-severe-asthma-in-thailand-100618162","NCT07328035","Remission in Adults With Severe Asthma in Thailand","Inclusion Criteria:\n\n* severe asthma\n* age 18 years or older\n\nExclusion Criteria:\n\n* inability to perform spirometry or fractional exhaled nitric oxide (FeNO) test",{"count":53,"type":19},230,"The goal of this observational study is to determine the prevalence of remission among adults with severe asthma, as well as the factors associated with remission in Thailand.\n\nThe main question the study aims to answer is:\n\nWhat is the prevalence of remission among adults with severe asthma in Thailand? Participants will complete questionnaires on asthma symptoms and undergo pulmonary function testing and a blood test once.",[56,57],"Severe Asthma","Asthma Control Level",[25,59,60,61,62,63],"remission","Thailand","severe","FeNO","blood eosinophil count","RECRUITING",{"date":66,"type":37},"2026-04-17",{"date":68,"type":37},"2026-01-01",{"date":41,"type":19},{"name":43,"class":44},1,{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":78,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":79,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":81,"conditions":82,"keywords":84,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":88,"startDateStruct":89,"completionDateStruct":91,"leadSponsor":93,"locationsCount":71},"100622459","chronic-obstructive-pulmonary-disease-and-asthma-in-workers-at-navanakorn-industrial-zone-thailand-100622459","NCT07383896","Chronic Obstructive Pulmonary Disease and Asthma in Workers at Navanakorn Industrial Zone, Thailand","Inclusion Criteria:\n\n* Age 18 years or older\n\nExclusion Criteria:\n\n* Inability to perform spirometry",true,{"count":80,"type":19},310,"The goal of this observational study is to determine the prevalence of asthma and chronic obstructive pulmonary disease (COPD) among workers in an industrial zone in Thailand.\n\nThe main question the study aims to answer is:\n\nWhat is the prevalence of asthma and COPD among workers in Thailand? Participants will complete a questionnaire on respiratory symptoms and undergo pulmonary function testing.",[23,83],"COPD",[25,83,27,85,86,60],"worker","industry","2026-04-15",{"date":66,"type":37},{"date":90,"type":37},"2025-09-01",{"date":92,"type":19},"2026-05-31",{"name":43,"class":44},{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":98,"acronym":4,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":100,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":102,"conditions":103,"keywords":105,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":113,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":117,"locationsCount":45},"100621878","comparative-study-of-cpap-predictive-equations-and-in-laboratory-manual-titration-in-thai-patients-with-obstructive-sleep-apnea-100621878","NCT07376343","Comparative Study of CPAP Predictive Equations and In-laboratory Manual Titration in Thai Patients With Obstructive Sleep Apnea","Inclusion Criteria:\n\n* Suspected OSA\n* Undergoing an in-laboratory sleep study\n\nExclusion Criteria:\n\n* No indication for in-laboratory manual CPAP titration\n* Failure to determine an optimal CPAP pressure during in-laboratory manual CPAP titration",{"count":101,"type":19},150,"The goal of this observational study is to compare predictive equations for continuous positive airway pressure (CPAP) with in-laboratory manual titration in patients with obstructive sleep apnea (OSA).\n\nThe main question the study aims to answer is:\n\nWhich CPAP predictive equation best predicts the optimal CPAP pressure in OSA patients in Thailand? Participants will undergo an in-laboratory sleep study.",[104],"OSA - Obstructive Sleep Apnea",[106,107,108,109,110,60,111,112],"OSA","obstructive sleep apnea","CPAP","continuous positive airway pressure","equation","sleep test","polysomnography",{"date":66,"type":37},{"date":115,"type":37},"2026-02-01",{"date":41,"type":19},{"name":43,"class":44},{"id":119,"slug":120,"hasResults":11,"nctId":121,"briefTitle":122,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":124,"targetDuration":4,"studyType":20,"phases":4,"briefSummary":126,"conditions":127,"keywords":129,"overallStatus":64,"whyStopped":4,"lastUpdateSubmitDate":87,"lastUpdatePostDateStruct":131,"startDateStruct":132,"completionDateStruct":133,"leadSponsor":134,"locationsCount":45},"100619999","remission-in-adults-with-mild-to-moderate-asthma-in-thailand-100619999","NCT07351916","Remission in Adults With Mild-to-moderate Asthma in Thailand","Inclusion Criteria:\n\n* mild-to-moderate asthma\n* age 18 years or older\n\nExclusion Criteria:\n\n* inability to perform spirometry or fractional exhaled nitric oxide (FeNO) test",{"count":125,"type":19},289,"The goal of this observational study is to determine the prevalence of remission among adults with mild-to-moderate asthma, as well as the factors associated with remission in Thailand.\n\nThe main question the study aims to answer is:\n\nWhat is the prevalence of remission among adults with severe asthma in Thailand? Participants will complete a questionnaire on asthma symptoms and undergo pulmonary function testing and a blood test once.",[23,128,57],"Mild-to-moderate Asthma",[25,26,130,60,59,62,63],"mild-to-moderate asthma",{"date":66,"type":37},{"date":115,"type":37},{"date":41,"type":19},{"name":43,"class":44},{"id":136,"slug":137,"hasResults":11,"nctId":138,"briefTitle":139,"officialTitle":140,"acronym":4,"eligibilityCriteria":141,"healthyVolunteers":11,"sex":15,"minAge":142,"maxAge":143,"enrollmentInfo":144,"targetDuration":4,"studyType":146,"phases":147,"briefSummary":149,"conditions":150,"keywords":153,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":160,"lastUpdatePostDateStruct":161,"startDateStruct":163,"completionDateStruct":165,"leadSponsor":167,"locationsCount":71},"100628580","preoperative-high-dose-oral-paracetamol-for-postoperative-analgesia-in-children-undergoing-tonsillectomy-100628580","NCT07463482","Preoperative High-Dose Oral Paracetamol for Postoperative Analgesia in Children Undergoing Tonsillectomy\"","Effect of Preoperative Oral Paracetamol Loading Dose Versus Standard Dose on Postoperative Opioid Consumption in Pediatric Tonsillectomy With Multimodal Analgesia: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Children aged 3 to 15 years\n2. ASA physical status I-III\n3. Scheduled for elective tonsillectomy with or without adenoidectomy\n\nExclusion Criteria:\n\n1. Known allergy or contraindication to paracetamol or any agents in the study protocol\n2. Chronic opioid use","3 Years","15 Years",{"count":145,"type":19},54,"INTERVENTIONAL",[148],"NA","This randomized clinical trial compares two different preoperative doses of oral paracetamol (acetaminophen) in children undergoing elective tonsillectomy. The aim is to determine whether a higher loading dose (30 mg\u002Fkg) decreases the need for opioid rescue medication after surgery compared with the standard dose (15 mg\u002Fkg), when used as part of a multimodal pain management approach. Children aged 3 to 15 years will be randomly assigned to receive either 30 mg\u002Fkg or 15 mg\u002Fkg of oral paracetamol before surgery. All participants will receive the same standard anesthesia and postoperative pain management. The primary outcome is the total amount of rescue opioid (fentanyl) required during the first 12 hours after surgery. Secondary outcomes include postoperative pain scores and the occurrence of side effects such as nausea and vomiting. This study seeks to determine whether a higher initial dose of paracetamol offers additional clinical benefits in pediatric tonsillectomy with multimodal analgesia.",[151,152],"Post Operative Analgesia","Tonsillectomy With or Without Adenoidectomy",[154,155,156,157,158,159],"paracetamol","acetaminophen","tonsillectomy","postoperative analgesia","pediatric anesthesia","multimodal analgesia","2026-03-05",{"date":162,"type":37},"2026-03-11",{"date":164,"type":19},"2026-03",{"date":166,"type":19},"2026-11",{"name":43,"class":44},{"id":169,"slug":170,"hasResults":11,"nctId":171,"briefTitle":172,"officialTitle":173,"acronym":174,"eligibilityCriteria":175,"healthyVolunteers":11,"sex":15,"minAge":176,"maxAge":177,"enrollmentInfo":178,"targetDuration":4,"studyType":146,"phases":180,"briefSummary":182,"conditions":183,"keywords":186,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":191,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":71},"100603745","phase-4-dinalbuphine-sebacate-in-postoperative-pain-control-after-tka-100603745","NCT07140510","Dinalbuphine Sebacate in Postoperative Pain Control After TKA","Effectiveness of Dinalbuphine Sebacate in Postoperative Pain Control Following Total Knee Arthroplasty: A Randomized Double Blinded Placebo-controlled Trial","Naldebain","Inclusion Criteria:\n\n* Osteoarthritic knee patients underwent unilateral primary TKA\n* Age 50-90 years\n* ASA class I-III\n* Participants understand and consent to the protocol of the trial\n\nExclusion Criteria:\n\n* Morbid obesity (BMI\\>40)\n* Knee osteoarthritis from inflammatory knee arthritis, trauma, infection\n* Previous knee surgery\n* Cognitive disorder\n* Liver disease\n* Allergy to NSAIDs, opioids, sesame oil, and benzyl benzoate\n* CYP3A4 inhibitor and inducer drugs used","50 Years","90 Years",{"count":179,"type":19},100,[181],"PHASE4","To evaluate the effectiveness of Dinalbuphine Sebacate for controlling subacute pain after total knee arthroplasty",[184,185],"Osteo Arthritis of the Knee","Total Knee Anthroplasty",[187,174,188,189,190],"Dinalbuphine Sebacate","Subacute pain","postoperative pain","total knee arthroplasty","2025-08-18",{"date":193,"type":37},"2025-08-24",{"date":195,"type":19},"2025-10",{"date":197,"type":19},"2026-09",{"name":43,"class":44},{"id":200,"slug":201,"hasResults":11,"nctId":202,"briefTitle":203,"officialTitle":204,"acronym":4,"eligibilityCriteria":205,"healthyVolunteers":11,"sex":15,"minAge":176,"maxAge":206,"enrollmentInfo":207,"targetDuration":4,"studyType":146,"phases":209,"briefSummary":210,"conditions":211,"keywords":214,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":225,"lastUpdatePostDateStruct":226,"startDateStruct":228,"completionDateStruct":230,"leadSponsor":232,"locationsCount":45},"100580309","comparison-of-functional-recovery-between-restricted-inverse-kinematic-alignment-and-adjusted-mechanical-alignment-with-robotic-assisted-unilateral-total-knee-arthroplasty-100580309","NCT06835621","Comparison of Functional Recovery Between Restricted Inverse Kinematic Alignment and Adjusted Mechanical Alignment With Robotic-assisted Unilateral Total Knee Arthroplasty.","Comparison of Functional Recovery Between Restricted Inverse Kinematic Alignment and Adjusted Mechanical Alignment With Robotic-assisted Unilateral Total Knee Arthroplasty. A Randomized Controlled Trial.","Inclusion Criteria:\n\n* Age 50 - 80 years old\n* Diagnosed with primary OA knee and indicated for unilateral total knee arthroplasty with MAKO robotic-assisted knee replacement system\n* ASA classification I-II\n\nExclusion Criteria:\n\n* Valgus deformity\n* KL grading \\> 3 on contralateral knee\n* Unable or difficulty for walking due to comorbidities\n* BMI \\> 40 kg\u002Fm2\n* Previous knee surgery\n* Infection around the knee","80 Years",{"count":208,"type":19},80,[148],"The goal of this clinical trial is to learn if restricted inverse kinematic alignment total knee arthroplasty (restricted iKA TKA) improves functional recovery compared to adjusted mechanical alignment total knee arthroplasty (aMA TKA) in patients undergoing unilateral robotic-assisted total knee arthroplasty by comparing performance-based outcome, 2-minute walk test (2MWT) as a primary outcome. This trial will also assess other outcomes including satisfaction, patient-reported functional outcomes, range of motion, visual analog scale for pain and complication of both techniques. The main question aims to answer is:\n\nIn unilateral robotic-assisted total knee arthroplasty, dose Restricted iKA technique provide better postoperative performance-based outcome compared to aMA technique?\n\nResearchers will compare restricted iKA and aMA technique to determine which technique offers better acceleration in functional recovery and patient satisfaction.\n\nParticipants will:\n\nAfter randomization, participants will allocate to either restricted iKA or aMA technique for unilateral robotic-assisted total knee arthroplasty.\n\nAttend follow-up visits for assessments of 2-minute walk test (Primary outcome), Time up and go test (TUG), VAS for pain, ROM and complete patient-reported functional outcome questionnaires regarding knee function and satisfaction at regular intervals.",[212,213],"OA Knee","TKA",[215,216,217,218,219,220,221,222,223,224],"Osteoarthritis (OA) of the Knee","OA knee","MAKO","Kinematic alignment","Mechanical alignment","Restricted Kinematic alignment","Inversed Kinematic alignment","Inversed Restricted Kinematic alignment","Robotic assist Total Knee Arthroplasty","Adjusted mechanical alignment","2025-02-14",{"date":227,"type":37},"2025-02-19",{"date":229,"type":19},"2025-03",{"date":231,"type":19},"2028-08",{"name":43,"class":44},""]