[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"vasectomy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:vasectomy":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,75],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":31,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100627625","vasectomy-right-for-me-decision-support-tool-100627625",false,"NCT07451067","\"Vasectomy: Right for Me?\" Decision Support Tool","Addressing Factors Related to Disparities in Vasectomy","Inclusion Criteria:\n\n* Are assigned male at birth\n* 21-55 years of age\n* Comfortable reading in English or Spanish\n* Live in the United States\n* Are considering vasectomy\n* Have not had a vasectomy\n\nExclusion Criteria:\n\n* Are not assigned male at birth\n* Are less than 21 or more than 55 years of age\n* Is not comfortable reading English nor Spanish\n* Do not live in the United States\n* Are not considering vasectomy\n* Have had a vasectomy\n* Once a racial or economic sub-group recruitment number has been reached, no other subjects fitting that ethnicity or income group will be enrolled.","MALE","21 Years","55 Years",{"count":20,"type":21},750,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of this trial is to learn if a web-based decision aid designed to provide evidence-based information about vasectomy and other birth control options helps improve users' decision-making about birth control. The main questions it aims to answer are:\n\n* Do people who use the decision aid have better knowledge about vasectomy?\n* Do people who use the decision aid have lower conflict with their decision?\n\nParticipants will:\n\n* Use the decision aid (if they are assigned to the intervention arm).\n* Answer survey questions about their knowledge, decision-making, interest in vasectomy, and healthcare navigation experiences.",[27,28,29,30],"Vasectomy","Contraception","Contraception Behavior","Reproductive Behavior",[27,32],"Decision aid","RECRUITING","2026-06-29",{"date":36,"type":37},"2026-07-01","ACTUAL",{"date":39,"type":37},"2026-06-20",{"date":41,"type":21},"2027-08",{"name":43,"class":44},"University of Pittsburgh","OTHER",2,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":4,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":16,"minAge":54,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":63,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":65,"lastUpdatePostDateStruct":66,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":74},"100597183","perioperative-virtual-reality-intervention-for-pain-and-anxiety-during-vasectomies-100597183","NCT07055178","Perioperative Virtual Reality Intervention for Pain and Anxiety During Vasectomies","A Perioperative Virtual Reality Intervention for Pain and Anxiety Management During Vasectomies: A Randomized Controlled Trial","Inclusion Criteria:\n\n* 18 years of age or older.\n* Can speak and read English.\n* Have elected for a vasectomy.\n* Are scheduled to undergo their vasectomy under local anesthesia at the Men's Health Clinic\n\nExclusion Criteria:\n\n* Those who are not competent to provide informed consent (e.g., due to cognitive impairment).\n* Those who are unable to participate in a VR intervention (e.g., due to visual or auditory impairment).",true,"18 Years",{"count":56,"type":21},90,[24],"The goal of this clinical trial is to learn if a virtual reality (VR) program (TRIPP) can reduce pain, anxiety, and distress in adult men (aged 18+) undergoing a vasectomy under local anesthesia. The main questions it aims to answer are:\n\n* Does using VR during a vasectomy lower patients' pain during the procedure compared to standard care?\n* Does VR reduce anxiety and distress compared to standard care?\n* Are patients more satisfied with their experience when using VR compared to standard care?\n\nResearchers will compare two groups:\n\n* VR group: Patients will use a VR headset with a guided meditation program (TRIPP) during their vasectomy.\n* Control group: Patients will receive standard care (no VR).\n\nParticipants will:\n\n* Be randomly assigned to either the VR group or control group.\n* Complete brief questionnaires before, during, and after the procedure (about 15-20 minutes each time).\n* (VR group only) Use a VR headset during the procedure and provide optional feedback about the experience.\n\nWhy is this important? Vasectomies are typically done with local anesthesia (pain relief), but many patients still feel anxiety or discomfort. VR may help distract and relax patients, improving their experience. This study will help health professionals understand if VR could be a useful option for future patients.",[27,60,61,62],"Pain","Anxiety","Virtual Reality",[62,64,27],"TRIPP","2026-04-28",{"date":67,"type":37},"2026-05-05",{"date":69,"type":37},"2025-07-02",{"date":71,"type":21},"2026-08",{"name":73,"class":44},"University of Manitoba",1,{"id":76,"slug":77,"hasResults":11,"nctId":78,"briefTitle":79,"officialTitle":80,"acronym":4,"eligibilityCriteria":81,"healthyVolunteers":11,"sex":16,"minAge":54,"maxAge":82,"enrollmentInfo":83,"targetDuration":4,"studyType":22,"phases":85,"briefSummary":87,"conditions":88,"keywords":89,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":92,"lastUpdatePostDateStruct":93,"startDateStruct":95,"completionDateStruct":97,"leadSponsor":99,"locationsCount":74},"100611826","early-phase-1-a-trial-of-self-adjusted-nitrous-versus-placebo-during-office-vasectomy-100611826","NCT07245628","A Trial of Self-Adjusted Nitrous Versus Placebo During Office Vasectomy","A Single-Blind Randomized Placebo Controlled Trial of Self-Adjusted Nitrous Oxide During Office Vasectomy","Inclusion Criteria:\n\n* Age 18 - 85 at the time of screening\n* Desiring vasectomy for family planning purposes\n* Able to understand and complete patient questionnaires\n* Willing and able to provide written consent to participate in the study\n\nExclusion Criteria:\n\n* Patients with unilateral absence of the vas deferens\n* Patients who are deemed by study surgeons to have anatomy no amendable for office procedure\n* Patients who decline office vasectomy and request monitored anesthesia care\n* Patients taking benzodiazepine or narcotic medication daily or within 24 hours of the procedure\n* Patients with contraindications to nitrous oxide including:\n* Inner ear, bariatric, or eye surgery within the past 2 weeks\n* Current emphysematous blebs\n* Severe B-12 deficiency\n* History of bleomycin chemotherapy within the last year\n* Class III or higher heart failure","85 Years",{"count":84,"type":21},50,[86],"EARLY_PHASE1","The goal of this clinical trial is to see if nitrous oxide is safe and effective to use during during vasectomies performed in a clinic\u002Fin-office setting.\n\nThis trial will compare self-administered nitrous oxide versus a placebo (oxygen) during office vasectomy.\n\nThe main questions it aims to answer are:\n\n* Whether self-administered low dose (20-45%) nitrous oxide (SANO) reduces intraoperative anxiety and catastrophizing during office vasectomy.\n* To examine whether SANO reduces intraoperative pain or alters procedure duration, the rate of adverse events, or urologists' perception of ease and patient tolerance of the procedure.\n\nParticipants will be asked to complete multiple surveys pre-procedure, intra-procedure, and post-procedure.",[27],[27,90,91],"Nitrous Oxide","Men's Health","2025-11-17",{"date":94,"type":37},"2025-11-24",{"date":96,"type":37},"2025-10-20",{"date":98,"type":21},"2030-05-01",{"name":100,"class":44},"Alexandra J. Berger Eberhardt, MD"]