[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Boston Intelligent Medical Research Center, Shenzhen United Scheme Technology Co., Ltd.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":71},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":17,"sex":18,"minAge":19,"maxAge":20,"enrollmentInfo":21,"targetDuration":4,"studyType":24,"phases":25,"briefSummary":27,"conditions":28,"keywords":4,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100603102","reinforcement-learned-automated-anesthesia-systems-during-painless-abortion-100603102",false,"NCT07132151","Reinforcement Learned Automated Anesthesia Systems During Painless Abortion","Automated Anesthesia Systems for Painless Abortion (AAS-PA): a Multi-center, Randomized Controlled Trial","AAS-PA","Inclusion Criteria:\n\n* Age between 18-45 years\n* ASA status Ⅰ to Ⅱ\n* Diagnosed with early intrauterine pregnancy\n* Body mass index (BMI) between 18 to 28 kg\u002Fm2\n\nExclusion Criteria:\n\n* History of cardiac, hepatic, renal, or metabolic disorders (e.g., diabetes, hypertension, sleep apnea)\n* Known allergy to opioids or ciprofloxacin components\n* Cachexia\n* History of substance or alcohol abuse\n* ASA class III or higher\n* Participation in any other drug clinical trial within the past 3 months\n* Long-term use of sedative or analgesic medications\n* History of neurological disorders and convulsions",true,"FEMALE","18 Years","45 Years",{"count":22,"type":23},167,"ESTIMATED","INTERVENTIONAL",[26],"NA","This study compares the automated anesthesia systems for painless abortion (AAS-PA) with traditional anesthesia in painless abortions. It assesses intraoperative indicators (hypoxemia, injection pain, hypotension, hemodynamics, respiratory depression) and postoperative outcomes (nausea, dizziness, recovery time, satisfaction). The AAS-PA group uses AI-adjusted intravenous ciprofol based on real-time vital signs and sedation depth; the traditional group relies on manual anesthesia. The goal is to verify if AAS-PA safely manages sedation, meets painless standards, reduces adverse events, and improves experience, aiding optimized automated protocols.",[29,30,31],"Painless Abortion","Artificial Intelligence (AI)","Ciprofol","NOT_YET_RECRUITING","2025-08-18",{"date":35,"type":36},"2025-08-20","ACTUAL",{"date":38,"type":23},"2025-09-08",{"date":40,"type":23},"2027-11-08",{"name":42,"class":43},"Boston Intelligent Medical Research Center, Shenzhen United Scheme Technology Co., Ltd.","INDUSTRY",8,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":17,"sex":53,"minAge":19,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":24,"phases":57,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":70},"100581979","reinforcement-learned-automatic-anesthesia-system-during-painless-gastrointestinal-endoscopy-100581979","NCT06857344","Reinforcement Learned Automatic Anesthesia System During Painless Gastrointestinal Endoscopy","Automated Anesthesia System-Gastrointestinal Endoscopy (AAS-GE): a Reinforcement Learning Based Control for Anesthesia During Gastrointestinal Endoscopy","AAS-GE","Inclusion Criteria:\n\n* American Society of Anesthesiologists (ASA) physical status class I-II\n* Expected operation duration less than 1 hour\n\nExclusion Criteria:\n\n* History of cardiac, hepatic, renal, or metabolic disorders (e.g., diabetes, hypertension, sleep apnea)\n* Known allergy to opioids or ciprofloxacin components\n* Cachexia\n* Hypothermia; history of narcotic abuse; chronic alcoholism; obesity (BMI \\>30); patients with apnea\n* Current pregnancy or lactation\n* History of substance abuse or alcohol dependence\n* Participation in any other drug clinical trial within the past 3 months\n* Obesity (BMI \\>30 kg\u002Fm²)\n* Procedure termination due to gastric retention or inadequate bowel preparation","ALL","65 Years",{"count":56,"type":23},164,[26],"The goal of this clinical trial is to compare the performance difference between trained model and clinical professionals in anesthesia control during gastrointestinal endoscopy. The participants would include adults aged between 18-65 years old with ASA scores I-II. The main questions it aims to answer are:\n\n* Can AI model successfully and safely perform anesthesia during gastrointestinal endoscopy?\n* Researchers hypothesis that anesthesia performed by professionals is not inferior to those performed by AI model.\n\nThe researchers will compare the results of the AI group with the traditional group to see if both groups have similar success rates in performing anesthesia.\n\nParticipants will fast for 8 hours before the procedure, and drinking water will be prohibited for 2 hours after taking the intestinal purgatives.",[60],"Anesthesia Induction","RECRUITING","2025-08-12",{"date":64,"type":36},"2025-08-15",{"date":66,"type":36},"2025-05-01",{"date":68,"type":23},"2025-10-01",{"name":42,"class":43},5,""]