[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"post-operative-recovery\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:post-operative-recovery":97},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,49,78],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100624828","phase-3-intravenous-lidocaine-plus-port-site-ropivacaine-for-recovery-after-laparoscopic-surgery-100624828",false,"NCT07414706","Intravenous Lidocaine Plus Port-Site Ropivacaine for Recovery After Laparoscopic Surgery","Evaluation of Postoperative Recovery When Combining Intravenous Lidocaine With Ropivacaine Infiltrations in Colorectal Laparoscopic Surgery","LivQor","Inclusion Criteria:\n\n* Patient undergoing scheduled colorectal cancer surgery via laparoscopy.\n* Patient aged 18 years or older.\n* Informed consent obtained and signed.\n* Affiliation to a social security system.\n\nExclusion Criteria:\n\n* Allergy or contraindication to lidocaine or ropivacaine.\n* Allergy or contraindication to paracetamol, nefopam ketamine, propofol, dexamethasone, sufentanil, Celebrex or parecoxib, morphine derivatives, and colorectal surgery by laparotomy\n* Colorectal surgery with a non-cancerous indication.\n* Chronic preoperative pain (defined as persistent pain for more than 3 months).\n* Preoperative use of opioids or opioid derivatives.\n* Patients with psychiatric disorders.\n* Patients for whom self-assessment of pain using a self-reported scale cannot be performed (non-communicative, non-French speaking, etc.).\n* Pregnant or breastfeeding women.\n* Patients under guardianship, curatorship, or legal protection.","ALL","18 Years",{"count":20,"type":21},182,"ESTIMATED","INTERVENTIONAL",[24],"PHASE3","This randomized controlled trial evaluates whether perioperative intravenous lidocaine infusion, combined with port-site ropivacaine infiltration, improves postoperative recovery after laparoscopic abdominal surgery. Participants will be assigned 1:1 to receive either intravenous lidocaine during surgery plus ropivacaine infiltration at surgical closure, or ropivacaine infiltration alone. The primary endpoint is postoperative quality of recovery measured by the QoR-15 questionnaire. Secondary endpoints include postoperative pain and opioid consumption, as well as plasma lidocaine and ropivacaine concentrations to assess systemic exposure and safety.",[27,28,29,30],"Intravenous Lidocaine","Laparoscopic Surgery","Post Operative Recovery","Local Anaesthetic Systemic Toxicity",[32,33,34,35],"Intravenous lidocaine","laparoscopic surgery","post operative recovery","local anaesthetic systemic toxicity","NOT_YET_RECRUITING","2026-02-12",{"date":39,"type":40},"2026-02-17","ACTUAL",{"date":42,"type":21},"2026-03",{"date":44,"type":21},"2028-09",{"name":46,"class":47},"Centre Hospitalier Universitaire, Amiens","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":55,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":22,"phases":59,"briefSummary":61,"conditions":62,"keywords":66,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":48},"100596360","digital-follow-up-program-after-discharge-home-following-thoracic-surgery-100596360","NCT07044440","Digital Follow-up Program After Discharge Home Following Thoracic Surgery","The Development and Evaluation of a Digital Follow-up Program During the Initial Four Weeks After Discharge Home Following Thoracic Surgery. A Confirmatory, Single-center, Prospective, Non-blinded, Randomized, Controlled Study","DFP","Inclusion Criteria:\n\n* Patients who have signed an informed consent form and underwent a surgery performed at the Thoracic Surgery Department of the University Hospital Basel\n* Age ≥ 18 years at the time of informed consent\n* First participation in the Study\n* Patient operated under general anesthesia\n* Patients who are in possession of a smart phone or personal computer and have an e-mail account and are able to answer a digital questionnaire. Or an immediate caretaker in the same household owns a smartphone or personal computer and is familiar with the use\n* Patients who understand verbal and written German or French\n* Patients discharged at home after surgery\n* Hospital stay \\> 3 nights after surgery\n\nExclusion Criteria:\n\n* Patients under preoperative opioid\u002Fcortisone therapy\n* Patients who are unable to follow the procedure of the study, e. g. read or understand German or French, psychological disorders, dementia, etc.\n* Enrolment of the investigator, his\u002Fher family members, employees and other dependent person\n* Patients with polytrauma or who underwent mediastinoscopy",{"count":58,"type":21},200,[60],"NA","The aim of the study is to evaluate whether a digital follow-up program can improve postoperative pain management and quality of life in patients during the first 28 days after discharge home following thoracic surgery, compared to standard follow-up care.",[63,64,29,65],"Thoracic Surgery","Mobile Health","Follow-up",[67,63],"Electronic Follow-up","RECRUITING","2025-08-04",{"date":71,"type":40},"2025-08-05",{"date":73,"type":40},"2025-07-30",{"date":75,"type":21},"2026-06",{"name":77,"class":47},"University Hospital, Basel, Switzerland",{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":85,"sex":86,"minAge":18,"maxAge":4,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":4,"overallStatus":68,"whyStopped":4,"lastUpdateSubmitDate":98,"lastUpdatePostDateStruct":99,"startDateStruct":101,"completionDateStruct":103,"leadSponsor":105,"locationsCount":48},"100554837","low-versus-standard-pressure-pneumoperitoneum-on-shoulder-tip-pain-100554837","NCT06504277","Low Versus Standard Pressure Pneumoperitoneum on Shoulder Tip Pain","A Randomized Controlled Trial (RCT) Comparing the Effect of Low Versus Standard Pressure Pneumoperitoneum on Post-operative Shoulder Tip Pain in Patients Undergoing Laparoscopic Gynecologic Surgery for Benign Indications","Inclusion Criteria: The participant must meet all of the inclusion criteria to eligible for this clinical trial:\n\n1. All ages \\> or = to 18 years old;\n2. Must be deemed to have capacity to provide informed consent;\n3. Must sign and date the informed consent form;\n4. Stated willingness to comply with all study procedures;\n5. Must be undergoing unilateral or bilateral salpingo-oopherectomy or salpingectomy or ovarian cystectomy;\n\nExclusion Criteria: An individual who meets any of the following criteria will be excluded from participation in this clinical trial:\n\n1. Previous midline laparotomy;\n2. Gynecological cancer beyond stage 1 disease;\n3. Chronic pain;\n4. Known diagnosis of endometriosis or evidence of endometriosis intra-operatively;\n5. Fibromyalgia;\n6. BMI \\>50;\n7. Language barrier;\n8. Inability to communicate or provide informed consent;",true,"FEMALE",{"count":88,"type":21},82,[60],"This proposed study is a single-center, double blind, parallel group RCT comparing the use of low (10 mm Hg) versus standard pressure (15 mm Hg) pneumoperitoneum at the time of benign gynecologic laparoscopic surgery. Patients will be randomized to the control group (standard pressure) or the intervention group (low pressure) and surgeons will be blinded to the study pressure. Data on post-operative recovery and pain scores will be recorded for each patient.",[92,93,94,95,96,97],"Surgery","Laparoscopic","Laparoscopy","Penumoperitoneum","Post-operative Pain","Post-operative Recovery","2025-07-28",{"date":100,"type":40},"2025-07-31",{"date":102,"type":40},"2025-07-02",{"date":104,"type":21},"2026-09-15",{"name":106,"class":47},"Mount Sinai Hospital, Canada"]