[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"perioperative-anesthetic\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:perioperative-anesthetic":27},{"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":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":40,"leadSponsor":42,"locationsCount":4},"100645160","effect-of-a-preoperative-educational-video-on-anxiety-levels-100645160",false,"NCT07679659","Effect of a Preoperative Educational Video on Anxiety Levels","Effect of QR Code-Based and Tablet-Based Preoperative Educational Video Interventions on Preoperative Anxiety","PEVA","Inclusion Criteria:\n\n* Age 18 years or older.\n* Scheduled for elective surgery under anesthesia.\n* Able to understand Turkish.\n* Able to provide written informed consent.\n\nExclusion Criteria:\n\n* Emergency surgery.\n* Visual or hearing impairment preventing video viewing.\n* Cognitive impairment.\n* Neurological or psychiatric disorders that may interfere with communication or completion of study questionnaires.","ALL","18 Years",{"count":20,"type":21},360,"ESTIMATED","INTERVENTIONAL",[24],"NA","Preoperative anxiety is common among patients undergoing elective surgery and may negatively affect perioperative outcomes. This randomized controlled trial aims to evaluate the effectiveness of a short educational video in reducing preoperative anxiety. Participants will be assigned to one of three groups: a QR code-based video group, a tablet-based video group, or a control group receiving standard preoperative information. Anxiety levels will be assessed using the Amsterdam Preoperative Anxiety and Information Scale (APAIS). The secondary objective is to evaluate the utilization of QR code-based video education.",[27,28],"Perioperative Anesthetic","Anxiety",[30,31,32,33],"Educational Video","Preoperative Anxiety","Patient Education","QR Code","NOT_YET_RECRUITING","2026-06-29",{"date":37,"type":38},"2026-07-01","ACTUAL",{"date":37,"type":21},{"date":41,"type":21},"2026-12-01",{"name":43,"class":44},"Aksaray University Training and Research Hospital","OTHER",{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":52,"minAge":18,"maxAge":53,"enrollmentInfo":54,"targetDuration":4,"studyType":22,"phases":56,"briefSummary":57,"conditions":58,"keywords":61,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"100640577","effects-of-rectal-indomethacin-suppository-on-postoperative-crbd-in-patients-undergoing-lrp-100640577","NCT07607990","Effects of Rectal Indomethacin Suppository on Postoperative CRBD in Patients Undergoing LRP","Effects of Rectal Indomethacin Suppository on Postoperative Catheter-Related Bladder Discomfort in Patients Undergoing Laparoscopic Radical Prostatectomy: A Randomized Controlled Trial","Inclusion Criteria:\n\n1. Aged 18 to 80 years old (inclusive);\n2. American Society of Anesthesiologists (ASA) physical status classification Class I-III;\n3. Undergoing elective laparoscopic radical prostatectomy under general anesthesia;\n4. Having a clear understanding of the study, voluntarily participating, and providing informed consent signed by themselves or their family members.\n\nExclusion Criteria:\n\n1. Pre-existing bladder diseases, such as overactive bladder (frequency of micturition \\> 3 times per night or \\> 8 times within 24 hours), neurogenic bladder, and bladder outlet obstruction;\n2. Postoperative status of pelvic organs or spine that affects bladder function;\n3. Postoperative status of total proctocolectomy;\n4. Severe cardiac insufficiency (activity tolerance \\\u003C 4 METs) or clearly diagnosed coronary heart disease;\n5. Clearly diagnosed chronic obstructive pulmonary disease (COPD) or a history of asthma;\n6. Hepatic insufficiency with Child-Pugh Class C;\n7. Chronic kidney disease requiring dialysis;\n8. Active peptic ulcer\u002Fhemorrhagic disease;\n9. Body mass index (BMI) ≤ 18 kg\u002Fm² or ≥ 28 kg\u002Fm²;\n10. Chronic analgesic abuse;\n11. Use of other nonsteroidal anti-inflammatory drugs (NSAIDs) within one week;\n12. Hypersensitivity to nonsteroidal anti-inflammatory drugs (NSAIDs);\n13. Mental or neurological disorders that prevent the completion of rating scales; or cognitive impairment resulting in the loss of capacity for civil conduct.","MALE","80 Years",{"count":55,"type":21},130,[24],"The postoperative incidence of catheter-related bladder discomfort (CRBD) ranges from 47% to 95%. It increases postoperative pain and agitation, thus requiring early intervention. Although a variety of drugs are used for the prevention or treatment of CRBD, the adverse reactions of most of these drugs have limited their clinical application. In long-term clinical practice, we found that indomethacin suppository has a good therapeutic effect on the discomfort of pelvic-related organs caused by nociceptive stimulation. However, its preventive effect on CRBD has not been reported yet. We hypothesized that indomethacin suppository has a preventive effect on postoperative CRBD. To verify this hypothesis, patients undergoing laparoscopic radical prostatectomy were enrolled in the study. Patients in the intervention group received 50 mg of indomethacin suppository via the rectal route immediately after surgery, while those in the control group received no treatment. The severity of CRBD, pain scores, consumption of analgesics, other perioperative adverse reactions, and patient satisfaction were observed and recorded at 0, 1, 2, and 6 hours after surgery.",[59,27,60],"Prostate Cancer (Post Prostatectomy)","Catheter-related Bladder Discomfort (CRBD)",[62,63,64],"catheter-related bladder discomfort","CRBD","radical prostatectomy","RECRUITING","2026-05-25",{"date":68,"type":38},"2026-05-27",{"date":70,"type":38},"2026-01-01",{"date":72,"type":21},"2026-12-31",{"name":74,"class":44},"Zhejiang University",1]