[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100639430":3},{"organization":4,"armGroups":7,"interventions":25,"overallOfficials":31,"centralContacts":31,"locations":40,"responsibleParty":51,"collaborators":31,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":31,"eligibilityCriteria":61,"healthyVolunteers":57,"sex":62,"minAge":63,"maxAge":64,"enrollmentInfo":65,"targetDuration":31,"studyType":68,"phases":69,"briefSummary":71,"conditions":72,"keywords":75,"overallStatus":77,"whyStopped":31,"lastUpdateSubmitDate":78,"lastUpdatePostDateStruct":79,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},{"fullName":5,"class":6},"Medipol University","OTHER",[8,14,19],{"label":9,"type":10,"description":11,"interventionNames":12},"Group QLB","EXPERIMENTAL","Patients will receive bilateral lateral Quadratus Lumborum Block (QLB) and port site infiltration at the end of the surgery.",[13],"Procedure: Lateral Quadratus Lumborum Block",{"label":15,"type":10,"description":16,"interventionNames":17},"Group TFP","Patients will receive bilateral Transversalis Fascia Plane (TFP) block and port site infiltration at the end of the surgery.",[18],"Procedure: Transversalis Fascia Plane Block",{"label":20,"type":21,"description":22,"interventionNames":23},"Group Control","ACTIVE_COMPARATOR","Patients will receive only port site infiltration at the end of the surgery.",[24],"Procedure: Port Site Infiltration",[26,32,36],{"type":27,"name":28,"description":29,"armGroupLabels":30,"otherNames":31},"PROCEDURE","Lateral Quadratus Lumborum Block","Bilateral ultrasound-guided lateral QLB with 20 mL of 0.25% bupivacaine per side (total 40 mL). Plus, 10 mL of 0.25% bupivacaine infiltration at trocar insertion sites.",[9],null,{"type":27,"name":33,"description":34,"armGroupLabels":35,"otherNames":31},"Transversalis Fascia Plane Block","Bilateral ultrasound-guided TFP block with 20 mL of 0.25% bupivacaine per side (total 40 mL). Plus, 10 mL of 0.25% bupivacaine infiltration at trocar insertion sites.",[15],{"type":27,"name":37,"description":38,"armGroupLabels":39,"otherNames":31},"Port Site Infiltration","Local infiltration of 20 mL of 0.25% bupivacaine at the trocar insertion sites.",[20],[41],{"facility":42,"status":31,"city":43,"state":31,"zip":31,"country":44,"countryCode":31,"cosmosGeoPoint":45,"geoPoint":50,"contacts":31},"Istanbul Medipol University","Istanbul","Turkey (Türkiye)",{"type":46,"coordinates":47},"Point",[48,49],28.94966,41.01384,{"lat":49,"lon":48},{"type":52,"investigatorFullName":53,"investigatorTitle":54,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"PRINCIPAL_INVESTIGATOR","Burak Omur","assist. prof.","100639430","comparison-of-qlb-and-tfp-block-for-postoperative-analgesia-in-laparoscopic-inguinal-hernia-100639430",false,"NCT07604259","Comparison of QLB and TFP Block for Postoperative Analgesia in Laparoscopic Inguinal Hernia","Comparison of the Effects of Ultrasound-Guided Lateral Quadratus Lumborum Block and Transversalis Fascia Plane Block on Postoperative Analgesia in Patients Undergoing Laparoscopic Inguinal Hernia Repair: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Scheduled for elective laparoscopic inguinal hernia repair.\n* American Society of Anesthesiologists (ASA) physical status I, II, or III.\n* Age between 18 and 65 years.\n* Provided written informed consent.\n\nExclusion Criteria:\n\n* History of allergy to local anesthetics.\n* Presence of coagulopathy.\n* Signs of infection at the intended block application site.\n* Body Mass Index (BMI) ≥ 35 kg\u002Fm².\n* History of chronic opioid use.\n* Presence of neurological disease.\n* Refusal to participate in the study.","ALL","18 Years","65 Years",{"count":66,"type":67},90,"ESTIMATED","INTERVENTIONAL",[70],"NA","This randomized controlled trial aims to compare the effects of ultrasound-guided lateral Quadratus Lumborum Block (QLB) and Transversalis Fascia Plane (TFP) block on postoperative analgesia in patients undergoing laparoscopic inguinal hernia repair. Ninety patients will be randomly assigned to one of three groups: Group QLB, Group TFP, or Group Control. The primary objective is to compare postoperative pain scores (NRS) at various time points within the first 24 hours. Secondary objectives include evaluating the need for rescue analgesia, total tramadol consumption, and the incidence of opioid-related side effects.",[73,74],"İnguinal Hernia","Post Operative Pain",[76],"Laparoscopic inguinal hernia, Quadratus Lumborum Block, Transversalis Fascia Plane Block, Postoperative analgesia, Regional anesthesia.","NOT_YET_RECRUITING","2026-05-18",{"date":80,"type":81},"2026-05-22","ACTUAL",{"date":83,"type":67},"2026-06-10",{"date":85,"type":67},"2027-05-10",{"name":5,"class":6},1]