[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100583775":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":31,"centralContacts":32,"locations":38,"responsibleParty":58,"collaborators":63,"id":67,"slug":68,"hasResults":69,"nctId":70,"briefTitle":71,"officialTitle":72,"acronym":31,"eligibilityCriteria":73,"healthyVolunteers":69,"sex":74,"minAge":75,"maxAge":31,"enrollmentInfo":76,"targetDuration":31,"studyType":79,"phases":80,"briefSummary":82,"conditions":83,"keywords":88,"overallStatus":41,"whyStopped":31,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":99,"completionDateStruct":101,"leadSponsor":103,"locationsCount":104},{"fullName":5,"class":6},"Lifespan","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Sublocade","ACTIVE_COMPARATOR","Participants receive Sublocade-branded injectable buprenorphine.",[13],"Drug: Sublocade",{"label":15,"type":10,"description":16,"interventionNames":17},"Brixadi","Participants receive Brixadi-branded injectable buprenorphine.",[18],"Drug: Brixadi (Injectable Buprenorphine)",[20,28],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Brixadi (Injectable Buprenorphine)","Brixadi comes in several doses and can be administered on a weekly or monthly basis. For clinical reasons (i.e., each patient will already be on a stable dose of MOUD in a setting without significant illicit opioid use), the monthly injection will be used. The approximately equivalent to the 300mg Sublocade dose is 96mg of Brixadi. The maximum dose is 128mg. Brixadi can be administered in the abdomen, buttocks, or triceps. Participants in the Brixadi treatment arm will be given one or more Brixadi injections each month prior to release from prison and each month after release. They can continue to receive the medication after the conclusion of the trial. Brixadi is covered by most Medicaid health insurances in the state of Rhode Island.",[15],[26,27],"CAM2308","Buvidal",{"type":21,"name":9,"description":29,"armGroupLabels":30,"otherNames":31},"Sublocade is a 100mg or 300mg pre-mixed subcutaneous injectable formulation to be administered monthly. Participants in the Sublocade treatment arm will be given monthly Sublocade injections, as clinically indicated, each month prior to release from prison and each month after release. They can continue to receive the medication after the conclusion of the trial. Sublocade is covered by most Medicaid health insurances in the state of Rhode Island. The standard dosing schedule is two months of 300mg followed by monthly 100mg injections. To maximize real-world generalizability, the medication dosing will be determined by clinical indication of the provider who will have the flexibility to provide medication dosing based on their clinical acumen and\u002For shared decision-making.",[9],null,[33],{"name":34,"role":35,"phone":36,"phoneExt":31,"email":37},"Justin Berk, MD MPH MBA","CONTACT","(401) 680-1074","justin_berk@brown.edu",[39],{"facility":40,"status":41,"city":42,"state":43,"zip":44,"country":45,"countryCode":46,"cosmosGeoPoint":47,"geoPoint":52,"contacts":53},"Rhode Island Department of Corrections","RECRUITING","Cranston","Rhode Island","02920","United States","US",{"type":48,"coordinates":49},"Point",[50,51],-71.43728,41.77982,{"lat":51,"lon":50},[54],{"name":55,"role":35,"phone":56,"phoneExt":31,"email":57},"Jessica Miggliacio","401-462-6721","Jessica.Migliaccio@doc.ri.gov",{"type":59,"investigatorFullName":60,"investigatorTitle":61,"investigatorAffiliation":62,"oldNameTitle":31,"oldOrganization":31},"PRINCIPAL_INVESTIGATOR","Justin Berk","Associate Professor","Rhode Island Hospital",[64],{"name":65,"class":66},"National Institute on Drug Abuse (NIDA)","NIH","100583775","phase-4-injectable-buprenorphine-in-prison-a-preference-trial-100583775",false,"NCT06880718","Injectable Buprenorphine in Prison: A Preference Trial","Injectable Buprenorphine During Transition Out of Prison: A Partially Randomized Preference Pilot Trial","Inclusion Criteria:\n\n1. be at least 18 years of age and incarcerated in the RIDOC facility,\n2. be currently diagnosed with OUD and enrolled in the RIDOC MOUD program,\n3. have an expected release date within 120 days of study enrollment,\n4. have an interest in XR-B and\n5. be English speaking\n\nExclusion Criteria:\n\n1. individuals who are pregnant or planning conception,\n2. diagnosed with a severe or acute medical or psychiatric disability preventing safe study participation or making follow-up unlikely,\n3. have a release date within 21 days of initiation, or\n4. have previously had an allergy to buprenorphine. Post-enrollment exclusion will include individuals if there is a change in release date beyond the 120 days and therefore no longer meet original inclusion criteria. These individuals would return to usual MOUD care.","ALL","18 Years",{"count":77,"type":78},60,"ESTIMATED","INTERVENTIONAL",[81],"PHASE4","The goal of this pilot trial is to compare two branded extended-release buprenorphine (XR-B) formulations (Sublocade vs. Brixadi) to explore how they improve treatment retention after release from prison among incarcerated individuals with opioid use disorder (OUD) who are transitioning back into the community.\n\nThe main question it aims to answer are:\n\nHow do Sublocade and Brixadi compare in terms of feasibility, acceptability, and effectiveness? Does giving people a choice of medication affect how well they stay in treatment?\n\nUsing a partially randomized preference trial approach, there will be a comparison between participants who choose their XR-B formulation to those who are randomly assigned to see if patient preference influences treatment outcomes. The trial is a hybrid implementation-effectiveness trial.\n\nParticipants will:\n\n* Choose which medication they prefer or be randomly assigned if they don't have a preference.\n* Receive monthly injections of either Sublocade or Brixadi before and after release from prison.\n* Complete surveys and clinical assessments on treatment experience and acceptability.\n* Be monitored for treatment retention, opioid use, and adverse events for six months post-release.\n\nResearchers will compare the two treatments to see which one works better for people leaving prison and if allowing people to choose their treatment improves results.",[84,85,86,87],"Opioid Use Disorder","Incarceration","Medications for Opioid Use Disorder","Buprenorphine",[89,90,91,92,93,94],"opioid use disorder","incarceration","prison","long-acting injectable","buprenorphine","XR-B","2026-05-13",{"date":97,"type":98},"2026-05-15","ACTUAL",{"date":100,"type":98},"2026-02-18",{"date":102,"type":78},"2027-06",{"name":5,"class":6},1]