[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"laparoscopic-abdominal-surgery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:laparoscopic-abdominal-surgery":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,43,66,94],{"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":4,"briefSummary":22,"conditions":23,"keywords":28,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100595208","comparison-of-short--and-long-term-outcomes-between-robotic-and-laparoscopic-hemicolectomy-of-right-colon-cancer--a-multicenter-propensity-score-matching-analysis-100595208",false,"NCT07029464","Comparison of Short- and Long-term Outcomes Between Robotic and Laparoscopic Hemicolectomy of Right Colon Cancer : A Multicenter Propensity Score Matching Analysis","Inclusion Criteria:\n\n* 1.Underwent radical right hemicolectomy by Da Vinci robotic or laparoscopic surgery 2.Postoperative pathology confirmed right colon adenocarcinoma (pT2-T4aNxM0; including cecal adenocarcinoma, ascending colon adenocarcinoma, hepatic flexure colon adenocarcinoma, and proximal transverse colon adenocarcinoma) 3.Complete clinical data and pathological results available\n\nExclusion Criteria:\n\n* 1.Received neoadjuvant therapy prior to surgery 2.History of other malignancies in the past 5 years (except cured cervical carcinoma in situ, basal cell carcinoma, or squamous cell carcinoma of the skin) 3.Distant metastases (e.g., liver, lung) or extensive abdominal\u002Fpelvic metastases confirmed by contrast-enhanced CT, PET-CT, or intraoperative exploration 4.Comorbid neurological\u002Fpsychiatric disorders impairing ability to express informed consent 5.Poor systemic condition with contraindications to general anesthesia 6.Severe obesity (BMI \\>35 kg\u002Fm²) 7.Severe widespread abdominal adhesions precluding safe pneumoperitoneum establishment 8.Emergency surgery due to tumor perforation or obstruction 9.Refusal to provide informed consent","ALL","18 Years","80 Years",{"count":19,"type":20},4000,"ESTIMATED","OBSERVATIONAL","This is a retrospective, multicenter cohort study to compare short- and long-term outcomes between robotic and laparoscopic hemicolectomy of right colon cancer.",[24,25,26,27],"Robotic Surgical Procedures","Right Colon Tumors","Cancer","Laparoscopic Abdominal Surgery",[29,30],"right colon cancer","robotic surgery","NOT_YET_RECRUITING","2025-06-17",{"date":34,"type":35},"2025-06-19","ACTUAL",{"date":37,"type":20},"2025-06",{"date":39,"type":20},"2027-05",{"name":41,"class":42},"The First Affiliated Hospital of Nanchang University","OTHER",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":60,"completionDateStruct":62,"leadSponsor":64,"locationsCount":4},"100575458","study-on-the-effects-of-multimodal-analgesia-regimens-on-postoperative-analgesia-and-gastrointestinal-function-recovery-after-laparoscopic-abdominal-surgery-100575458","NCT06772545","Study on the Effects of Multimodal Analgesia Regimens on Postoperative Analgesia and Gastrointestinal Function Recovery After Laparoscopic Abdominal Surgery","A Prospective Comparative Study on the Effects of Multimodal Analgesia Regimens on Postoperative Analgesia and Gastrointestinal Function Recovery After Laparoscopic Abdominal Surgery","Inclusion Criteria:\n\n* \\>18 years old\n* ASA I-III\n* Ability to understand and voluntarily sign the informed consent form\n* No prior use of long-acting or addictive analgesic drugs before surgery.\n\nExclusion Criteria:\n\n* History of previous abdominal surgery\n* Presence of severe cardiovascular, respiratory, hepatic, renal, neurological, or psychiatric disorders\n* Pre-existing chronic pain conditions\n* Known allergy to any analgesic drugs used in this study\n* Presence of spinal deformities, neurological conditions, or coagulopathy that may affect the performance of regional anesthesia.\n* Pregnant or breastfeeding women\n* Inability to cooperate with study procedures or understand pain rating scales\n* History of opioid abuse or addiction.",{"count":51,"type":20},120,"INTERVENTIONAL",[54],"NA","This clinical trial aims to investigate the impact of multimodal analgesia regimens on postoperative pain management and gastrointestinal function recovery following laparoscopic abdominal surgery. The primary objectives are to determine:\n\nWhich analgesic regimen is most effective in reducing postoperative pain? Which analgesic regimen is most effective in accelerating gastrointestinal function recovery? This study will compare epidural analgesia (EA), paravertebral block (PB), transversus abdominis plane block (TAP), and patient-controlled intravenous analgesia (PCIA) to identify the optimal method for pain control and the most beneficial for gastrointestinal recovery.\n\nParticipants will receive one of the following treatments postoperatively: epidural analgesia, paravertebral block, TAP block, or patient-controlled intravenous analgesia. Rest pain (measured using the Numerical Rating Scale, NRS), dynamic pain (NRS), morphine equivalent consumption (mg), quality of sleep on the first night (Likert scale, 1-5), time to return of bowel function (h), time to recommence oral intake (h), time to first mobilization (h), quality of recovery (QoR, 0-15) on postoperative day 1, and length of hospital stay (days) will be recorded at 4, 8, 12, and 24 hours post-procedure.",[27],"2025-01-12",{"date":59,"type":35},"2025-01-14",{"date":61,"type":20},"2025-02-01",{"date":63,"type":20},"2025-05-10",{"name":65,"class":42},"Xiaguang Duan",{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":74,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":75,"targetDuration":4,"studyType":52,"phases":77,"briefSummary":78,"conditions":79,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":93},"100568666","the-impact-of-a-dexmedetomidine-perfusion-on-intraoperative-remifentanil-consumption-100568666","NCT06684197","The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption","The Impact of a Dexmedetomidine Perfusion on Intraoperative Remifentanil Consumption: a Randomized Controlled Trial","DEXREM","Inclusion Criteria:\n\n* ASA 1-3\n* Laparascopic surgery (including general surgery, gynecology, urology) a small abdominal incision (less than 5 cm) will be tolerated.\n\nExclusion Criteria:\n\n* Patient refusal\n* Chronic use of opioids\n* Allergy to medication used in the trial\n* Pregnant or breastfeeding women\n* Contraindications to dexmedetomidine (Bradycardia, arrythmia or pace- maker, severe ventricular dysfunction)",true,{"count":76,"type":20},72,[54],"Opioids analgesic are the gold standard for intraoperative pain management. Their short- and long-term adverse effect motivate anesthesiologists to explore opioid sparing strategies. Dexmedetomidine is a highly selective α2 adrenergic receptor agonist that could help minimize opioid consumption both intraoperative and postoperative due to its sedative, analgesic and sympatholytic properties. This new randomized controlled trial (RCT) will answer the question whether an intraoperative dexmedetomidine infusion compared to placebo has a clinically significant impact on intraoperative remifentanil consumption during a laparoscopic abdominal elective surgery.",[80,81,82,83,27],"Dexmedetomidine","Total Intravenous Anesthesia","Remifentanil Consumption","Remifentanil","2024-11-08",{"date":86,"type":35},"2024-11-12",{"date":88,"type":20},"2024-11",{"date":90,"type":20},"2025-11",{"name":92,"class":42},"Ciusss de L'Est de l'Île de Montréal",1,{"id":95,"slug":96,"hasResults":11,"nctId":97,"briefTitle":98,"officialTitle":98,"acronym":99,"eligibilityCriteria":100,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":101,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":103,"conditions":104,"keywords":105,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":111,"lastUpdatePostDateStruct":112,"startDateStruct":114,"completionDateStruct":116,"leadSponsor":118,"locationsCount":120},"100566497","outcome-related-performance-evaluation-through-revision-and-analysis-of-intraoperative-events-100566497","NCT06655948","Outcome-related Performance Evaluation Through Revision and Analysis of inTraoperative Events","OPERATE","Inclusion Criteria:\n\n* Patients scheduled for elective minimally-invasive surgery in participating centers\n* Patients with no contraindication to anesthesia and laparoscopic procedures\n* Capable of providing informed consent\n\nExclusion Criteria:\n\n* Surgery performed with palliative intent or under unplanned\u002Femergency setting\n* Pregnant or breastfeeding patient\n* Patient under legal custody or guardianship",{"count":102,"type":20},700,"The goal of this prospective, multicentric, observational, cohort study is to evaluate intraoperative adverse events (iAEs) through video-based assessment (VBA) across minimal invasive procedures performed in general surgery departments. The main questions it aims to answer are:\n\n* The prevalence, type, and severity of iAEs\n* Correlation between iAE and clinical outcomes\n* Correlation between iAE and surgical performance\n* Qualitative analysis of root cause analysis and mitigation strategies",[27],[106,107,108,109,110],"Intraoperative Adverse Events","Video-Based Assessment","Minimally Invasive Surgery","Surgical Performance","Patient Outcomes","2024-10-22",{"date":113,"type":35},"2024-10-24",{"date":115,"type":20},"2024-10",{"date":117,"type":20},"2029-10",{"name":119,"class":42},"Fondazione Policlinico Universitario Agostino Gemelli IRCCS",5]