[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100548877":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":31,"centralContacts":35,"locations":44,"responsibleParty":66,"collaborators":26,"id":69,"slug":70,"hasResults":71,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":26,"eligibilityCriteria":75,"healthyVolunteers":71,"sex":76,"minAge":77,"maxAge":78,"enrollmentInfo":79,"targetDuration":26,"studyType":82,"phases":83,"briefSummary":85,"conditions":86,"keywords":89,"overallStatus":47,"whyStopped":26,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":98,"leadSponsor":100,"locationsCount":101},{"fullName":5,"class":6},"Koç University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Group S","EXPERIMENTAL","Participants who will be receiving a serratus posterior superior intercostal plane block with a single dose of 30 ml of %0,25 bupivacaine",[13],"Procedure: Serratus Posterior Superior Intercostal Plane Block",{"label":15,"type":16,"description":17,"interventionNames":18},"Group P","ACTIVE_COMPARATOR","Participants who will be receiving a thoracal paravertebral block with a single dose of 30 ml of %0,25 bupivacaine",[19],"Procedure: Paravertebral Block",[21,27],{"type":22,"name":23,"description":24,"armGroupLabels":25,"otherNames":26},"PROCEDURE","Serratus Posterior Superior Intercostal Plane Block","Before the induction of general anesthesia, under aseptic conditions, serratus posterior superior intercostal plane block will be performed with a single dose of 30 ml of %0,25 bupivacaine with ultrasound guidance, by the senior anaesthesiologist.",[9],null,{"type":22,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Paravertebral Block","Before the induction of general anesthesia, under aseptic conditions, paravertebral block will be performed with a single dose of 30 ml of %0,25 bupivacaine with ultrasound guidance, by the senior anaesthesiologist.",[15],[32],{"name":33,"affiliation":5,"role":34},"Kamil Darçın, MD","PRINCIPAL_INVESTIGATOR",[36,40],{"name":33,"role":37,"phone":38,"phoneExt":26,"email":39},"CONTACT","+90 505 589 50 99","drdarcink@gmail.com",{"name":41,"role":37,"phone":42,"phoneExt":26,"email":43},"Yasemin Sincer, MD","+90 531 204 08 34","sincer.yasemin@gmail.com",[45],{"facility":46,"status":47,"city":48,"state":26,"zip":49,"country":50,"countryCode":26,"cosmosGeoPoint":51,"geoPoint":56,"contacts":57},"Koc University","RECRUITING","Istanbul","34010","Turkey (Türkiye)",{"type":52,"coordinates":53},"Point",[54,55],28.94966,41.01384,{"lat":55,"lon":54},[58,62,65],{"name":59,"role":37,"phone":60,"phoneExt":26,"email":61},"Kamil Darçın","+905055895099","kdarcin@ku.edu.tr",{"name":63,"role":37,"phone":64,"phoneExt":26,"email":43},"Yasemin Sincer","+90512040834",{"name":59,"role":34,"phone":26,"phoneExt":26,"email":26},{"type":34,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":26,"oldOrganization":26},"Kamil Darcin","MD","100548877","tpvb-or-spsipb-in-pain-management-after-vats-100548877",false,"NCT06426706","TPVB or SPSIPB in Pain Management After VATS","Paravertebral Block or Serratus Posterior Superior Intercostal Plane Block in Pain Management After Video-Assisted Thoracoscopic Surgery: A Randomized Controlled Clinical Trial","Inclusion Criteria:\n\n* Patients between the age of 18-80 undergoing video-assisted thoracoscopic surgery\n\nExclusion Criteria:\n\n* Allergy to local anaesthetics Chronic opioid use history Patients with psychiatric disorders Patients who are not open to communication Patients with chronic organ failure Patients that do not give consent Patients that need emergency surgery within the first 24 hours of the initial surgery","ALL","18 Years","80 Years",{"count":80,"type":81},44,"ESTIMATED","INTERVENTIONAL",[84],"NA","The goal of this clinical trial is to compare the analgesic efficacy of thoracal paravertebral block (TPVB) and serratus posterior superior intercostal plane block (SPSIPB) in patients undergoing video-assisted thoracoscopic surgery (VATS). The main questions it aims to answer are:\n\nHow will the total perioperative opioid consumption of the patients receiving two different blocks change? How will TPVB and SPSIPB effect the patients' numeric rating scores for pain in the postoperative 24-hour period? How will TPVB and SPSIPB effect the incidence of opioid related side effects?\n\nParticipants will be divided in two groups:\n\nTPVB group will receive a TPVB before the surgery. SPSIPB group will receive a SPSIPB nerve block before the surgery. Researchers will compare the results between the groups to see the postoperative effects concerning opioid consumption as well as the pain scores, respiratory parameters and opioid associated side effects.\n\nThe hypothesis of this study is that participants receiving SPSIPB for VATS will have a less total opioid consumption 24 hours postoperatively.",[87,28,23,88],"Video-assisted Thoracoscopic Surgery","Regional Anesthesia Morbidity",[90,91,92],"video-assisted thoracoscopic surgery","paravertebral block","serratus posterior superior intercostal plane block","2025-01-02",{"date":95,"type":96},"2025-01-03","ACTUAL",{"date":95,"type":81},{"date":99,"type":81},"2025-03-15",{"name":5,"class":6},1]