[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"validity\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:validity":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,46,68,94],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":31,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100592243","comparison-of-the-analgesic-effect-of-oliceridine-versus-morphine-or-sufentanil-for-postoperative-analgesia-in-lumbar-surgeries-a-randomized-control-trial-100592243",false,"NCT06990893","Comparison of the Analgesic Effect of Oliceridine Versus Morphine or Sufentanil for Postoperative Analgesia in Lumbar Surgeries: a Randomized Control Trial","Inclusion Criteria:\n\n* Lumbar spine surgery with ASA grades I-III\n* Aged 18-65 years\n* Ethically, the patient voluntarily accepted this trial and signed the informed consent form\n\nExclusion Criteria:\n\n* Severe respiratory and circulatory system diseases\n* Nervous system disease\n* Mental and psychological disorders\n* Abnormal liver and kidney functions\n* Participated in another drug clinical research within the past 30 days","ALL","18 Years","65 Years",{"count":19,"type":20},90,"ESTIMATED","INTERVENTIONAL",[23],"NA","Objective: This study aimed to compare the efficacy and safety of oliceridine versus morphine and sufentanil for postoperative analgesia following elective lumbar spine surgery.\n\nMethods: In this randomized, controlled trial, 90 patients scheduled for lumbar spine surgery were allocated in a 1:1:1 ratio to receive postoperative intravenous patient-controlled analgesia (PCIA) with either oliceridine (Group O，1.5mg oliceridine for loading dose， 0.5mg\u002Fkg oliceridine for PICA), morphine (Group M，4mg morphine for loading dose，1.5mg\u002Fkg morphine for PICA), or sufentanil (Group S，4ug sufentanil for loading dose，1.5ug\u002Fkg sufentanil for PICA). The primary outcome was the movement Visual Analogue Scale (VAS) score at 6 hours postoperatively. Secondary outcomes included resting and movement VAS scores, ramsay sation score at 0.5, 2, 6, 12, 24, and 48 hours postoperatively (excluding the motor VAS score at 6 hours postoperatively); number of PCIA demands and rescue analgesic requirements within 48 hours; hemodynamic parameters at 5, 10, 15, 30, and 60 minutes after administration of the initial loading dose. The incidence of adverse events within 48 hours postoperatively, such as nausea and vomiting, somnolence, respiratory depression, or pruritus.",[26,27,28,29,30],"Sufentanil","Morphine","Validity","Safety","Oliceridine",[26,29,27,32],"oliceridine","RECRUITING","2026-05-28",{"date":36,"type":37},"2026-06-01","ACTUAL",{"date":39,"type":37},"2025-06-01",{"date":41,"type":20},"2026-10-01",{"name":43,"class":44},"Anqing Municipal Hospital","OTHER",1,{"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":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":45},"100598593","the-validity-of-the-evaluation-of-renal-artery-duplex-in-critically-ill-acute-kidney-injury-patients-100598593","NCT07073508","The Validity of the Evaluation of Renal Artery Duplex in Critically Ill Acute Kidney Injury Patients","Inclusion Criteria:\n\n* Patients age \\>18 years.\n* Both sexes.\n* Patients within 24 hours after intensive care unit (ICU) admission.\n\nExclusion Criteria:\n\n* Patients presented with poor abdominal echogenicity.\n* Chronic kidney disease, especially with estimated creatinine clearance less than 30 ml\u002Fmin\u002F1.73m.\n* Patients with dialysis dependency.\n* Patients with renal transplantation.\n* Patients with known renal artery stenosis.\n* If there is a pregnancy.\n* Patients with any congenital kidney diseases as mono-kidney, anatomic kidney abnormalities.",{"count":53,"type":20},100,"OBSERVATIONAL","This study aims to assess the clinical relevance of renal artery duplex ultrasound in critically ill patients with acute kidney injury (AKI) in terms of the renal resistive index (RRI).",[28,57,58],"Renal Artery Duplex","Critically Ill Acute Kidney Injury","2025-07-10",{"date":61,"type":37},"2025-07-18",{"date":63,"type":37},"2024-05-01",{"date":65,"type":20},"2026-05-01",{"name":67,"class":44},"Ain Shams University",{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":15,"minAge":75,"maxAge":76,"enrollmentInfo":77,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":79,"conditions":80,"keywords":4,"overallStatus":84,"whyStopped":4,"lastUpdateSubmitDate":85,"lastUpdatePostDateStruct":86,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":45},"100566482","craniocervical-dysfunction-index-in-patients-with-temporomandibular-joint-dysfunction-100566482","NCT06655753","Craniocervical Dysfunction Index in Patients With Temporomandibular Joint Dysfunction","Turkish Validity and Reliability of the Craniocervical Dysfunction Index in Patients Temporomandibular Joint Dysfunction","Inclusion Criteria:\n\n* Between the ages of 20-60 years\n* Clinical diagnosis of non-specific neck pain\n* Being able to communicate in Turkish\n* Volunteering to participate in the study\n\nExclusion Criteria:\n\n* Over 60 years of age\n* Those with impairments in cervical mobility that affected the postural assessment","20 Years","60 Years",{"count":78,"type":20},50,"The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with Temporomandibular Joint Dysfunction, reliability and validity of the index Turkish speaking adults.",[81,82,83,28],"Temporomandibular Joint Dysfunction","Craniocervical Dysfunction","Reliability","NOT_YET_RECRUITING","2025-02-07",{"date":87,"type":37},"2025-02-11",{"date":89,"type":20},"2025-03-01",{"date":91,"type":20},"2025-10-01",{"name":93,"class":44},"Alanya Alaaddin Keykubat University",{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":99,"acronym":4,"eligibilityCriteria":100,"healthyVolunteers":101,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":102,"targetDuration":4,"studyType":54,"phases":4,"briefSummary":104,"conditions":105,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":45},"100520282","turkish-version-of-digital-eye-strain-questionnaire-desq-100520282","NCT06054542","Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Validity and Reliability of the Turkish Version of Digital Eye Strain Questionnaire (DESQ)","Inclusion Criteria:\n\n* Between the ages of 18-65 years\n* People who spend two or more continuous hours a day on their digital devices (computer, tablet, smartphone) or use more than one device\n\nExclusion Criteria:\n\n* History of ophthalmic surgery or active ocular disease\n* Participants who did not understand the instructions or did not sign a consent form were excluded",true,{"count":103,"type":20},130,"The aims of this study were to perform cultural adaptation of the DESQ and provide information regarding the factor structure, reliability and validity of the instrument in Turkish speaking adults.",[106,83,28,107,108],"Cultural Adaptation","Adults","Eye Strain","2024-10-11",{"date":111,"type":37},"2024-10-15",{"date":113,"type":37},"2023-10-30",{"date":115,"type":20},"2024-12",{"name":93,"class":44}]