[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Andrea Saporito\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":112},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,47,84],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":46},"100619887","pushes-pudendal-block-versus-sacral-esp-hemorrhoidectomy-study-100619887",false,"NCT07350460","PUSHES (Pudendal Block Versus Sacral ESP Hemorrhoidectomy Study)","A Randomized, Double-Blind Trial Comparing Pudendal Block Versus Sacral ESP for Ambulatory Hemorrhoidectomy","PUSHES","Inclusion Criteria:\n\n* Adults (≥18 years old) scheduled for elective excisional hemorrhoidectomy;\n* Ability to understand the nature of the study and provide written informed consent;\n* American Society of Anesthesiologists (ASA) physical status I-III;\n* Ability to comply with study procedures and postoperative evaluations.\n\nExclusion Criteria:\n\n* Pregnancy;\n* Body weight under 50 kg due to the potential risk of local anaesthetic systemic toxicity (LAST);\n* BMI \\> 40; Known allergy or contraindication to local anaesthetics (e.g., ropivacaine, prilocaine);\n* Severe coagulation disorders or current anticoagulant therapy contraindicating spinal or peripheral deep nerve blocks (like pudendal block, because Sacral ESP is considered a superficial block);\n* Infection at the puncture site;\n* Neurological disorders affecting the sacral or pudendal nerve pathways;\n* Severe psychiatric conditions impairing study participation;\n* Language barriers","ALL","18 Years","80 Years",{"count":21,"type":22},64,"ESTIMATED","INTERVENTIONAL",[25],"NA","The goal of this clinical trial is to learn if the sacral erector spinae plane block can provide equal or better pain control than the pudendal nerve block in adults undergoing hemorrhoid surgery. The main question is: Which block offers more effective analgesia and faster recovery?",[28,29],"Hemorrhoids","Hemorrhoids Third Degree",[28,31,32,33],"Hemorrhoidectomy","Postoperative Pain","Pain Measurement","RECRUITING","2026-03-16",{"date":37,"type":38},"2026-03-18","ACTUAL",{"date":40,"type":38},"2026-01-05",{"date":42,"type":22},"2027-09-30",{"name":44,"class":45},"Andrea Saporito","OTHER",1,{"id":48,"slug":49,"hasResults":11,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":55,"enrollmentInfo":56,"targetDuration":4,"studyType":23,"phases":58,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":83,"locationsCount":46},"100606455","teleconsultation-vs-face-to-face-evaluation-for-perioperative-respiratory-events-in-pediatric-adenotonsillectomy-100606455","NCT07175779","Teleconsultation vs Face-to-Face Evaluation for Perioperative Respiratory Events in Pediatric Adenotonsillectomy","Effect of Teleconsultation Compared to Face-to-Face Evaluation on Perioperative Respiratory Events in Pediatric Adenotonsillectomy: A Randomized Non Inferiority Trial","Teleped","Inclusion Criteria:\n\n* Pediatric patients (up to 16 years of age) undergoing elective tonsillectomy or adenotonsillectomy\n* ASA (American Society of Anesthesiologists) physical status I to III,\n* Patients who have a parent or legal guardian able and willing to provide informed consent.\n\nExclusion Criteria:\n\n* Parent or guardian unable or unwilling to provide informed consent,\n* Refusal to participate by parent\u002Fguardian,\n* Patients with contraindications to general anesthesia,\n* Known allergy to any drugs used in the anesthetic protocol.\n* Potential difficult airway,\n* Poorly controlled chronic illness (e.g. asthma),\n* Cardiac disease ,\n* Genetic disorder,\n* Haemoglobinopathy, anemia or clotting problem,\n* Complex physical disability,\n* Request from the patient or carer","16 Years",{"count":57,"type":22},106,[25],"The goal of this clinical trial is to assess whether preoperative anesthesia teleconsultation is at least equivalent to in-person consultation in preventing perioperative respiratory adverse events (such temporary reduction in oxygen levels in the blood) in the operating room and in the first 24 hours after the surgery in pediatric adenotonsillectomy.\n\nResearchers will compare the teleconsultation to in-person consultation to see if there is a difference in the frequency of respiratory adverse events in the operating room and during the first 24 hours after adenotonsillectomy.\n\nParticipants will:\n\n\\- undergo a traditional in-person anesthesiology consultation scheduled at the hospital or a online preoperative anesthesiology teleconsultation.",[61],"Adenotonsillar Hypertrophy",[63,64,65,66,67,68,69,70,71,72,73,74,75,76],"Anesthesia Consultation","Face-to-Face Visit","Remote consultation","Patient anxiety","Patient Satisfaction","Lost Work Time","Distance Traveled","Virtual Care","Digital Health","Telemedicine","Perioperative Care","Perioperative respiratory adverse events (PRAE)","Adenotonsillectomy","Tonsillectomy","2026-03-13",{"date":35,"type":38},{"date":80,"type":38},"2025-12-11",{"date":82,"type":22},"2027-05",{"name":44,"class":45},{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":4,"eligibilityCriteria":90,"healthyVolunteers":11,"sex":91,"minAge":18,"maxAge":4,"enrollmentInfo":92,"targetDuration":4,"studyType":23,"phases":94,"briefSummary":95,"conditions":96,"keywords":99,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":110,"locationsCount":111},"100565474","evaluation-and-comparison-between-general-anesthesia-vs-two-types-of-combined-anesthesia-for-opioid-consumption-in-laparoscopic-hysterectomy-100565474","NCT06642649","Evaluation and Comparison Between General Anesthesia VS Two Types of Combined Anesthesia for Opioid Consumption in Laparoscopic Hysterectomy","Evaluation and Comparison Between General Anesthesia VS Two Types of Combined Anesthesia (general and Spinal Anesthesia) for Opioid Consumption in Laparoscopic Hysterectomy: a Multi-Center, Randomized, Prospective, Controlled Trial","Inclusion Criteria:\n\n* patients over 18 year of age,\n* ASA physical status I to III scheduled for laparoscopic hysterectomy (with or without adnexectomy)\n\nExclusion Criteria:\n\n* patients with inability to consent,\n* patient refusal,\n* contraindication to spinal anesthesia (e.g., hemodynamic instability, infection at the surgery site, and neurologic defects such as transverse myelitis, coagulopathies or ongoing anticoagulant therapy),\n* known chronic pain syndrome, known\n* suspected non- compliance,\n* drug, or alcohol abuse ,\n* major oncological surgeries,\n* allergy to drugs used in the protocol,\n* previous chronic use of analgesics\n* history of opioid abuse","FEMALE",{"count":93,"type":22},45,[25],"The aim of the study is to evaluate and compare general anesthesia VS two types of combined anesthesia in opioid consumption after laparoscopic hysterectomy",[97,98],"Laparoscopic Hysterectomy","Gynecology",[100,101,102],"laparoscopic hysterectomy","spinal anesthesia","general anesthesia","2025-02-26",{"date":105,"type":38},"2025-02-28",{"date":107,"type":38},"2024-11-01",{"date":109,"type":22},"2026-04-30",{"name":44,"class":45},2,""]