[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sanliurfa Education and Research Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":154},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,50,77,103,127],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100632151","effect-of-preoperative-erector-spinae-plane-block-on-recovery-quality-time-to-return-to-daily-activities-and-postoperative-pain-scores-in-inguinal-hernia-surgery-100632151",false,"NCT07509957","Effect of Preoperative Erector Spinae Plane Block on Recovery Quality, Time to Return to Daily Activities, and Postoperative Pain Scores in Inguinal Hernia Surgery","ESPB for IHR","Inclusion Criteria:\n\n1. Patients aged between 18 and 65 years\n2. Patients scheduled to undergo open IHT surgery under spinal anesthesia (unilateral)\n3. Both male and female patients\n\nExclusion Criteria:\n\n1. Patients with coagulation disorders\n2. Patients with chronic opioid use\n3. Patients who develop intraoperative complications\n4. Patients with a preoperative Numeric Rating Scale (NRS) pain score ≥4\n5. Patients with a history of revision (recurrent) surgery\n6. Patients unable to communicate for any reason\n7. Patients who decline to participate in the study","ALL","18 Years","65 Years",{"count":20,"type":21},60,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study aims to evaluate the effect of the erector spinae plane block (ESPB), performed after surgery, on quality of recovery, postoperative pain, and time to return to daily activities in patients undergoing open inguinal hernia repair under spinal anesthesia.\n\nPostoperative pain following inguinal hernia surgery may delay recovery and negatively affect patients' return to normal daily life. Although ESPB has been widely used as an effective analgesic technique in various surgical procedures, its effectiveness in inguinal hernia repair remains limited and not well established.\n\nIn this randomized controlled study, patients will be divided into two groups: one group will receive ESPB after surgery, while the control group will not receive any block. All patients will receive standard postoperative analgesia.\n\nQuality of recovery, acute pain scores, and analgesic consumption will be assessed within the first 24 hours after surgery, and return to daily activities will be evaluated 30 days after surgery.\n\nThe primary outcome of this study is quality of recovery assessed using the Quality of Recovery-15 (QoR-15) questionnaire. QoR-15 scores range from 0 to 150, with higher scores indicating better recovery. Scores will be recorded preoperatively and 24 hours after surgery.\n\nSecondary outcomes include postoperative pain intensity, total opioid consumption, and time to return to daily activities. Pain intensity will be assessed using the Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst pain imaginable, at 15, 30, 60, and 120 minutes, as well as 6, 12, and 24 hours after surgery.\n\nTotal opioid consumption will be determined by recording the cumulative dose of intravenous tramadol administered as rescue analgesia within the first 24 hours after surgery. Time to return to daily activities will be evaluated via telephone follow-up 30 days after surgery.",[27,28,29,30,31],"Inguinal Hernia Unilateral","Erector Spinae Plane Block","Quality of Recovery (QoR-15)","Numeric Rating Scale","Return to Daily Activity",[33,28,34,35,31,36],"Inguinal Hernia Repair","Regionel Anesthesia","Quality of Recovery","Postoperative Pain","RECRUITING","2026-07-01",{"date":40,"type":41},"2026-07-02","ACTUAL",{"date":43,"type":41},"2026-04-04",{"date":45,"type":21},"2026-07-16",{"name":47,"class":48},"Sanliurfa Education and Research Hospital","OTHER_GOV",2,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":54,"acronym":4,"eligibilityCriteria":55,"healthyVolunteers":56,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":60,"conditions":61,"keywords":65,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":76},"100635022","comparison-of-the-effects-of-external-oblique-intercostal-plane-block-and-subcostal-transversus-plane-block-methods-with-ultrasound-guidance-on-postoperative-analgesia-in-laparoscopic-sleeve-gastrectomy-operations-100635022","NCT07547280","Comparison of the Effects of External Oblique Intercostal Plane Block and Subcostal Transversus Plane Block Methods With Ultrasound Guidance on Postoperative Analgesia in Laparoscopic Sleeve Gastrectomy Operations","Inclusion Criteria:\n\n* Adult patients aged between 18 and 65 years\n* Patients classified as American Society of Anesthesiologists (ASA) physical status I-III\n\nExclusion Criteria:\n\n* Patients younger than 18 years or older than 65 years\n* Inability to cooperate or comply with study procedures\n* Liver and kidney failure\n* American Society of Anesthesiologists (ASA) IV-V patient\n* External oblique intercostal block(EOİB) and the Subcostal Transversus Abdominis Plane block(s-TAB) are contraindicated",true,{"count":58,"type":21},90,[24],"The primary aim of this study was to investigate the effects of the external oblique intercostal plane block and the subcostal transversus abdominis plane block on postoperative pain scores and opioid consumption in patients undergoing laparoscopic sleeve gastrectomy.",[62,63,64],"Sleeve Gastrectomy","External Oblique Intercostal Plane Block","Subcostal Transverse Abdominis Plane Block",[66],"Ultrasound guided · External oblique intercostal plane block · Sleeve gastrectomy Bariatric surgery Postoperative · Analgesia","NOT_YET_RECRUITING","2026-04-20",{"date":70,"type":41},"2026-04-23",{"date":72,"type":21},"2026-04-01",{"date":74,"type":21},"2027-05-01",{"name":47,"class":48},1,{"id":78,"slug":79,"hasResults":11,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":83,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":85,"targetDuration":4,"studyType":86,"phases":4,"briefSummary":87,"conditions":88,"keywords":91,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":99,"completionDateStruct":100,"leadSponsor":102,"locationsCount":76},"100632980","clinical-outcomes-after-laser-hemorrhoidoplasty-100632980","NCT07520734","Clinical Outcomes After Laser Hemorrhoidoplasty","Clinical Outcomes, Pain Scores, and Patient Satisfaction in Patients Undergoing Laser Hemorrhoidoplasty: A Prospective Observational Study","LHP","Inclusion Criteria:\n\n* Age 18 years or older\n* Symptomatic internal hemorrhoidal disease\n* Scheduled to undergo laser hemorrhoidoplasty\n* Willingness to participate and provision of informed consent\n\nExclusion Criteria:\n\n* Grade IV hemorrhoidal disease\n* Acute thrombosed hemorrhoids\n* Additional anorectal pathology such as anal fissure, fistula, or perianal abscess\n* History of inflammatory bowel disease or colorectal malignancy\n* Previous major anal surgery'",{"count":20,"type":21},"OBSERVATIONAL","This single-center prospective observational study aims to evaluate clinical outcomes, postoperative pain scores, complications, and patient satisfaction in adults undergoing laser hemorrhoidoplasty for symptomatic internal hemorrhoidal disease. Additional objectives are to assess the relationship between hemorrhoid stage, dominant presenting symptoms, operative technical details, and postoperative outcomes. No study-specific intervention beyond routine clinical care and follow-up will be performed.",[89,90],"Hemorrhoidal Disease","Internal Hemorrhoids",[92,93,94,95],"Laser hemorrhoidoplasty","Hemorrhoidal disease","Patient satisfaction","Visual Analog Scale","2026-04-02",{"date":98,"type":41},"2026-04-09",{"date":72,"type":21},{"date":101,"type":21},"2027-04-01",{"name":47,"class":48},{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":111,"targetDuration":4,"studyType":86,"phases":4,"briefSummary":113,"conditions":114,"keywords":116,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":122,"completionDateStruct":124,"leadSponsor":126,"locationsCount":76},"100631134","comparison-of-diagnostic-methods-in-patients-operated-for-suspected-appendicitis-100631134","NCT07496723","Comparison of Diagnostic Methods in Patients Operated for Suspected Appendicitis","Prospective Evaluation of the Impact of Computed Tomography Reporting and AIR Scoring System on Negative Appendectomy Rates in Patients With Acute Appendicitis","APP-AIR","Inclusion Criteria:\n\n* Age 18 years or older\n* Presentation to the emergency department with suspected acute appendicitis\n* Underwent computed tomography after clinical evaluation\n* Computed tomography report compatible with acute appendicitis\n* Underwent appendectomy for presumed acute appendicitis\n* Provided informed consent\n\nExclusion Criteria:\n\n* Age younger than 18 years\n* Pregnancy\n* Planned additional surgical intervention in the same session for a reason other than appendicitis\n* Intraoperative finding of a non-appendiceal pathology requiring a different surgical procedure\n* Refusal to participate in the study",{"count":112,"type":21},200,"Acute appendicitis is one of the most common surgical emergencies, but diagnostic uncertainty may still lead to unnecessary appendectomy in some patients. This prospective observational study aims to evaluate the diagnostic performance of computed tomography (CT) reporting and the Appendicitis Inflammatory Response (AIR) score in adult patients undergoing appendectomy for suspected acute appendicitis. The primary objective is to determine the negative appendectomy rate based on final histopathology. Secondary objectives are to assess the agreement between AIR score, CT findings, intraoperative severity grading, and pathology results, and to explore diagnostic performance across patient subgroups. No study-specific intervention beyond routine clinical care will be performed.",[115],"Acute Appendicitis",[117,118,119],"Appendicitis Inflammatory Response Score","Appendectomy","Computed Tomography","2026-03-26",{"date":72,"type":41},{"date":123,"type":41},"2026-03-18",{"date":125,"type":21},"2027-01-31",{"name":47,"class":48},{"id":128,"slug":129,"hasResults":11,"nctId":130,"briefTitle":131,"officialTitle":132,"acronym":133,"eligibilityCriteria":134,"healthyVolunteers":11,"sex":135,"minAge":17,"maxAge":136,"enrollmentInfo":137,"targetDuration":4,"studyType":22,"phases":139,"briefSummary":140,"conditions":141,"keywords":143,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":147,"lastUpdatePostDateStruct":148,"startDateStruct":150,"completionDateStruct":151,"leadSponsor":153,"locationsCount":4},"100580733","prediction-of-adhesion-by-sliding-sign-100580733","NCT06841146","Prediction of Adhesion by Sliding Sign","Prediction of Adhesion by Sliding Sign in Three or Above Cesarean Section","Prediction","Inclusion Criteria:\n\n* all three and above number of cesarean section patients\n\nExclusion Criteria: placenta adhesion spectrum\n\n\\-","FEMALE","50 Years",{"count":138,"type":21},100,[24],"Sliding sign will be checked by ultrasonography by transabdominal and transvaginal route before operation of patients that had cesarean section three or more. During cesarean section adhesions will be evaluated and noted. The correlation and predictive values of adhesion and sliding sign will be defined in our study.",[142],"Adhesions Abdominal",[144,145,146],"adhesion","cesarean section","sliding sign","2025-02-19",{"date":149,"type":41},"2025-02-24",{"date":147,"type":21},{"date":152,"type":21},"2025-03-31",{"name":47,"class":48},""]