[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"colonoscopy-procedure\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:colonoscopy-procedure":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":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":5},"100642139","phase-4-patient-controlled-propofol-sedation-versus-nurse-assisted-propofol-sedation-in-diagnostic-colonoscopies-with-a-focus-on-patient-satisfaction-100642139",false,"NCT07653867","Patient Controlled Propofol Sedation Versus Nurse-assisted Propofol Sedation in Diagnostic Colonoscopies With a Focus on Patient Satisfaction","Patient-Controlled Anesthesia for Endoscopic Procedural Sedation (PCAPS). A Randomized Controlled Trial Evaluating Patient-controlled Propofol Sedation in Diagnostic Colonoscopies","PCAPS1","Inclusion Criteria:\n\n* Scheduled for elective diagnostic colonoscopy in propofol sedation\n* Able to understand the study information and provide inform consent\n* ASA I-II\n* Able to understand and use the patient-controlled sedation device\n* Able to complete study quistioneeres\n\nExclusion Criteria:\n\n* ASA \\>=III\n* Known hypersensitivity or contraindication to propofol or any excipient in the formulation.\n* Pregnancy or breastfeeding.\n* Inability to provide valid informed consent\n* Cognitive impairment, severe psychiatric illness, or other condition limiting reliable participation or questionnaire completion.\n* Inability to understand study procedures or insufficient language proficiency without available validated study support.\n* History of serious adverse reaction or complication related to sedation or anesthesia.","ALL","18 Years","90 Years",{"count":21,"type":22},135,"ESTIMATED","INTERVENTIONAL",[25],"PHASE4","The goal of this clinical trial is to learn if patient administered propofol sedation results in superior patient satisfaction compared to nurse administered propofol sedation in diagnostic colonoscopies.\n\n• Does self administration of the sedative propofol increase patient satisfaction? Researchers will compare patient administered propofol sedation (where the patient administers propofol by pushing a button) with nurse administered propofol sedation (where a nurse gives the patient bolus doses of propofol as deemed necessary)\n\nParticipants will:\n\n* Be randomized to either sedation route.\n* Answer a preendoscopy questioneere and a postendoscopy questioneere 1 hour after the examination as well as one week after the examination.",[28],"Colonoscopy (Procedure)",[30,31,32],"colonoscopy","sedation","patient controlled propofol sedation","NOT_YET_RECRUITING","2026-06-16",{"date":36,"type":37},"2026-06-17","ACTUAL",{"date":39,"type":22},"2026-11-01",{"date":41,"type":22},"2028-11-01",{"name":43,"class":44},"Karolinska Institutet","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":17,"minAge":53,"maxAge":4,"enrollmentInfo":54,"targetDuration":4,"studyType":23,"phases":56,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":70},"100609868","use-of-gi-genius-xr-software-in-virtual-reality-headset-during-routine-colonoscopy-100609868","NCT07220174","Use of GI Genius™ XR Software in Virtual Reality Headset During Routine Colonoscopy","Pilot Usability Evaluation of GI Genius™ XR Software Running on a Virtual Reality Headset During Routine CRC Screening and Surveillance Colonoscopies","Inclusion Criteria for patient:\n\n* Male or female aged ≥ 45 years;\n* Scheduled for routine CRC screening or surveillance colonoscopy;\n* Written informed consent to participate.\n\nInclusion Criteria for endoscopist:\n\n* Male or female board-certified gastroenterologists experienced with CRC screening and surveillance colonoscopy;\n* Written informed consent to participate.\n\nExclusion Criteria for patient:\n\n* Not able to comply with the protocol requirement;\n* Implanted or worn medical device (pacemaker, defibrillator, insulin pump, etc.).\n\nExclusion Criteria for endoscopist:\n\n* Not able to comply with the protocol requirement;\n* Implanted or worn medical device (pacemaker, defibrillator, insulin pump, etc.);\n* Risk of falls;\n* Seizures;\n* Heart disease;\n* Pregnant;\n* Migraines;\n* Eye or vision disorder;\n* Inner ear disorder;\n* Psychological disorder.",true,"45 Years",{"count":55,"type":22},15,[57],"NA","This pilot study will evaluate the usability and safety of software GI Genius™ XR in the Apple Vision Pro™ virtual reality headset when used in conjunction with the GI Genius™ system during routine screening and surveillance colonoscopy procedures. GI Genius™ XR enables colonoscopists to view the standard live endoscopic video feed within a virtual reality environment as an alternative to the conventional endoscopy tower display. The system provides a virtual screen that mirrors the tower video output without any image analysis or interpretation, allowing users to adjust screen size and position for optimal visualization and situational awareness.",[28],"2025-10-21",{"date":62,"type":37},"2025-10-23",{"date":64,"type":22},"2025-10-31",{"date":66,"type":22},"2026-04",{"name":68,"class":69},"Cosmo Artificial Intelligence-AI Ltd","INDUSTRY",1,"Colonoscopy Procedure"]