[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Erzurum Regional Training & Research Hospital\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":111},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,44,68,92],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100616921","m-tapa-block-and-transversus-abdominal-plane-block-for-postoperative-analgesia-in-unilateral-open-inguinal-hernia-repair-surgery-100616921",false,"NCT07311902","M-Tapa Block and Transversus Abdominal Plane Block for Postoperative Analgesia in Unilateral Open Inguinal Hernia Repair Surgery","Comparison of Patient Satisfaction Survey and Pain Follow-up in Patients Who Underwent M-Tapa Block and Transversus Abdominal Plane Block for Postoperative Analgesia in Unilateral Open Inguinal Hernia Repair Surgery","pain","Exclusion Criteria:\n\n* History of bleeding diathesis\n* Allergy or sensitivity to local anesthetics and opioids\n* Infection in the area where the block will be applied\n* Alcohol or drug addiction\n* Patients with a BMI \\> 30\n* Suspected pregnancy\n* Women in pregnancy or lactation\n* Patients with allergies to study drugs\n* Patient refusal\n* Use of anticoagulant agents\n\nInclusion Criteria:\n\n* Planning for elective unilateral open inguinal hernia repair surgery\n* ASA I-II status\n* Being between 18 and 65 years of age","ALL","18 Years","65 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","Patients will be called to the operating room one hour before surgery and no premedication will be applied before coming to the operating room. Patients in both groups who are taken to the block room will be administered 1-2 mg iv midazolam for sedation. M TAPA block will be applied for the surgical procedure. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. The US probe will be placed in the saggital plane at the costochondral angle where the midclavicular line intersects the costal cartilage. 5 ml of saline will be injected using the in-plane technique using a 22G 100 mm block needle and the block location will be verified. After the block location is verified, a total of 20 ml of 0.25% bupivacaine will be injected unilaterally and the procedure will be terminated. After aseptic conditions are provided, the high-frequency linear US probe will be covered with a sterile sheath. In TAP block, the block needle will be advanced to the fascial plane between the internal oblique and transversus abdominis muscles with the in-plane technique and the procedure will be completed by injecting 5 ml 20 ml 0.25% bupivacaine unilaterally. The same analgesia protocol will be applied to both groups intraoperatively and postoperatively, and a survey will be conducted on the patients at the 24th hour postoperatively.",[28,29,30],"Pain Management","Mtapa Block","TAP Block","RECRUITING","2025-12-30",{"date":34,"type":35},"2025-12-31","ACTUAL",{"date":37,"type":35},"2024-11-01",{"date":39,"type":22},"2026-01-01",{"name":41,"class":42},"Erzurum Regional Training & Research Hospital","OTHER_GOV",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":50,"minAge":18,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":23,"phases":53,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":59,"lastUpdatePostDateStruct":60,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":67},"100448273","comparison-of-transversalis-fascia-plane-block-and-erector-spinae-plane-blocks-in-cesarean-section-100448273","NCT05117307","Comparison of Transversalis Fascia Plane Block and Erector Spinae Plane Blocks in Cesarean Section","Inclusion Criteria:\n\n* Between 18-50 years\n* Cesarean Section\n\nExclusion Criteria:\n\n* Cesarean Section under general anesthesia\n* emergency cases\n* those with a body mass index greater than 35 kg\u002Fm2\n* coagulopathy\n* local infection","FEMALE","50 Years",{"count":21,"type":22},[25],"Cesarean section is one of the most common major surgical procedures performed worldwide,, Post-cesarean analgesia should provide adequate pain control while allowing the mother to remain active to meet the needs of the baby. Insufficient analgesia after cesarean section may be associated with acute postoperative pain, chronic pain, higher opioid consumption, delayed functional capacity, and postpartum depression. Techniques such as neuraxial techniques, oral and intravenous agents, wound infiltration, and behavioral therapy can be used in the treatment of post-cesarean pain pain. In addition, Transversus abdominis plane block (TAP), Quadratus Lumborum block (QLB), Erector Spina block (ESP), Transversalis Fascia plane block (TFP) are used safely under ultrasound guidance. In this study, it was aimed primarily to examine the effects of TFP and ESP blocks on pain scores, and secondarily to evaluate analgesic consumption.",[56,57],"Pain","Postoperative Pain","NOT_YET_RECRUITING","2025-12-16",{"date":61,"type":35},"2025-12-22",{"date":63,"type":22},"2025-12-20",{"date":65,"type":22},"2026-06-30",{"name":41,"class":42},2,{"id":69,"slug":70,"hasResults":11,"nctId":71,"briefTitle":72,"officialTitle":73,"acronym":4,"eligibilityCriteria":74,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":75,"targetDuration":4,"studyType":23,"phases":77,"briefSummary":78,"conditions":79,"keywords":81,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":4},"100598650","blind-needling-accuracy-in-lumbar-muscles-100598650","NCT07074249","Blind Needling Accuracy in Lumbar Muscles","Anatomical Accuracy of Blind Dry Needling Procedures on the Lumbar Paraspinal Muscles: An Ultrasonography-Assisted Observational Study","Inclusion Criteria:\n\n* Adults aged 18-65\n\n  * Individuals with nonspecific low back or back pain and planned physical therapy\n  * Individuals with suspected MPS, especially in the paraspinal muscles\n  * Individuals with indications for dry needling\n  * Those who can cooperate with the procedure and give written consent\n\nExclusion Criteria:\n\n* \\* Anticoagulant use\n\n  * History of spine surgery, deformity, severe scoliosis\n  * Regional skin lesion or infection\n  * Patients who cannot cooperate\n  * Pregnancy\n  * Serious systemic diseases such as malignancy or neurological disease",{"count":76,"type":22},20,[25],"The aim of this study is to evaluate the accuracy of blinded invasive interventions (dry needling) on the deep paraspinal muscles of the lumbar region (iliocostalis lumborum, longissimus thoracis, and multifidus) to reach the anatomical target. The accuracy of the interventions will be evaluated observationally with ultrasonography after the procedure.",[80],"Dry Needling Lumbar Paraspinal Muscles",[82,83],"dry needling","ultrasound guidance","2025-09-18",{"date":86,"type":35},"2025-09-19",{"date":88,"type":22},"2025-09-28",{"date":90,"type":22},"2025-09-30",{"name":41,"class":42},{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":4,"eligibilityCriteria":98,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":99,"targetDuration":4,"studyType":23,"phases":101,"briefSummary":102,"conditions":103,"keywords":105,"overallStatus":58,"whyStopped":4,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":107,"startDateStruct":108,"completionDateStruct":109,"leadSponsor":110,"locationsCount":4},"100599018","can-we-reliably-needle-hip-muscles-blindly-100599018","NCT07079033","Can We Reliably Needle Hip Muscles Blindly?","Can We Reliably Needle Hip Region Muscles Without Imaging? A Muscle-Specific Accuracy Study Using Ultrasound","Inclusion Criteria:\n\n* Adults aged 18 to 65 years\n* Individuals with nonspecific hip, groin, or anterior thigh pain who are scheduled for physical therapy\n* Clinical suspicion of myofascial pain syndrome, particularly involving muscles around the hip\n* Patients with clinical indication for dry needling or similar invasive treatments (e.g., targeting muscles such as iliacus, pectineus, sartorius)\n* Ability to cooperate with the procedure\n* Ability to provide written informed consent\n\nExclusion Criteria:\n\n* Use of anticoagulant medications (due to increased risk of bleeding)\n* Severe hip osteoarthritis, presence of hip prosthesis, history of previous hip surgery, or significant anatomical deformity\n* Active infection or skin lesion at the planned injection site\n* Inability to cooperate or communicate effectively\n* Pregnancy\n* Presence of serious systemic illnesses (e.g., malignancy, neurological disorders)",{"count":100,"type":22},40,[25],"The aim of this study is to evaluate the accuracy of invasive interventions (dry needling or injection) performed on specific muscles of the hip region in reaching the anatomical target. The accuracy of the interventions performed with a blinded method will be compared with an observational assessment supported by ultrasonography. The interventions will be performed by a physician with clinical experience, and the anatomical location of the needle tip will be evaluated by a second physician with ultrasonography after each procedure. The targeted muscles include the iliacus, pectineus, sartorius, tensor fascia latae, and rectus femoris. Each participant will be subjected to interventions for five different muscles, and a total of at least 40 injection interventions will be analyzed. Ultrasonography will be used only for observation and verification purposes; no pharmacological substances will be applied during the procedure. All procedures will be performed under sterile conditions, and participants will be monitored for 24 hours for possible pain, bruising, or complications. Participants will be informed about the content and purpose of the study, and written informed consent forms will be obtained. The study does not have a therapeutic purpose and is only intended to investigate targeting accuracy. The data to be obtained is expected to contribute to the determination of anatomical accuracy rates in clinical practices and the improvement of interventional training processes.",[104],"Hip Needling",[82,106,83],"trigger point",{"date":86,"type":35},{"date":88,"type":22},{"date":90,"type":22},{"name":41,"class":42},""]