[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"shoulder-arthroscopy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:shoulder-arthroscopy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,51,72,103,130,157,182],{"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":30,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":4},"100651576","speng-block-versus-suprascapular-and-axillary-nerve-blocks-for-pain-after-shoulder-arthroscopy-100651576",false,"NCT07762417","SPENG Block Versus Suprascapular and Axillary Nerve Blocks for Pain After Shoulder Arthroscopy","Analgesic Efficacy of the Shoulder Posterior Pericapsular Nerve Group Block Versus Combined Posterior Suprascapular and Axillary Nerve Blocks for Shoulder Arthroscopy: A Randomized, Blinded, Non-Inferiority Trial","SPENG-RCT","Inclusion Criteria:\n\n* Age 18 to 70 years\n* American Society of Anesthesiologists (ASA) physical status I-III\n* Scheduled to undergo elective shoulder arthroscopy under general anesthesia\n* Able to understand the Numeric Rating Scale for pain assessment\n* Able and willing to provide written informed consent\n\nExclusion Criteria:\n\n* Known allergy or hypersensitivity to local anesthetics used in the study\n* Infection at the planned block injection site\n* Coagulopathy or ongoing anticoagulant therapy that cannot be appropriately interrupted for peripheral nerve block\n* Pre-existing neurological deficit affecting the operative upper extremity\n* Moderate or severe pulmonary disease\n* Known diaphragmatic dysfunction\n* Chronic opioid use\n* Chronic pain syndrome\n* Body mass index greater than 35 kg\u002Fm²\n* Pregnancy or breastfeeding\n* Inability to understand or reliably report Numeric Rating Scale pain scores\n* Inadequate sonographic window preventing safe performance of the allocated block technique before randomization","ALL","18 Years","70 Years",{"count":21,"type":22},60,"ESTIMATED","INTERVENTIONAL",[25],"NA","This prospective, randomized, patient- and assessor-blinded, single-center non-inferiority trial will compare the analgesic efficacy of the Shoulder Posterior Pericapsular Nerve Group (SPENG) block with combined posterior suprascapular and axillary nerve blocks in adults undergoing elective shoulder arthroscopy under general anesthesia. Both groups will receive the same total volume and concentration of local anesthetic. The primary outcome will be the highest resting Numeric Rating Scale pain score recorded during the first 24 postoperative hours. Secondary outcomes will include block performance time, sensory block success in suprascapular and axillary nerve territories, opioid consumption, time to rescue analgesia, motor function, diaphragmatic function, postoperative recovery quality, patient satisfaction, and block-related complications.",[28,29],"Postoperative Pain","Shoulder Arthroscopy",[31,32,33,34,35,36,37,38],"Diaphragm-sparing block","Postoperative analgesia","Regional anesthesia","Axillary nerve block","Suprascapular nerve block","Shoulder arthroscopy","Shoulder Posterior Pericapsular Nerve Group block","SPENG block","NOT_YET_RECRUITING","2026-08-12",{"date":42,"type":43},"2026-08-14","ACTUAL",{"date":45,"type":22},"2026-11-01",{"date":47,"type":22},"2027-06-15",{"name":49,"class":50},"Izmir City Hospital","OTHER_GOV",{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":57,"targetDuration":4,"studyType":23,"phases":59,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100648785","use-of-a-smartphone-app-to-support-pre--and-post-surgical-preparedness-and-to-improve-clinical-outcomes-in-patients-undergoing-shoulder-arthroscopy-100648785","NCT07725224","Use of a Smartphone App to Support Pre- and Post-Surgical Preparedness and to Improve Clinical Outcomes in Patients Undergoing Shoulder Arthroscopy","Inclusion Criteria:\n\n* scheduled for shoulder arthroscopy with participating surgeon\n\nExclusion Criteria:\n\n\\-",{"count":58,"type":22},100,[25],"This study is testing whether a smartphone app can help patients better follow instructions before and after shoulder surgery, compared to the usual paper instructions.\n\nPeople from all backgrounds sometimes have trouble understanding or remembering everything needed to prepare for surgery and recover safely - things like when to stop certain medications, how to shower with a special soap before surgery, or how to care for a wound afterward. Missing these steps can lead to surgery being delayed or canceled, or to problems during recovery. These difficulties can be greater for patients facing barriers such as limited health information, language differences, or lack of support at home.\n\nThis study includes adults having planned shoulder arthroscopy (a type of shoulder surgery) at Johns Hopkins. Participants will be randomly assigned to one of two groups: one will receive the standard printed instructions currently used in clinic, and the other will receive the same instructions through an app on the smartphone. The app also pulls basic information from the patient's electronic health record - surgery type, date, surgeon, and medications - so instructions can be tailored to each patient. Patients using the app confirm when each step is completed, such as taking a medication or showering before surgery, and also report on how the participant is doing after surgery, which is shared with the patient's care team.\n\nThe goal is to see whether the app helps patients follow instructions more closely, improves the patient's experience and recovery, and reduces the workload on nurses and clinic staff - particularly for patients who face more barriers to care.",[29],"2026-07-21",{"date":64,"type":43},"2026-07-24",{"date":66,"type":22},"2026-09-15",{"date":68,"type":22},"2028-03-31",{"name":70,"class":71},"Johns Hopkins University","OTHER",{"id":73,"slug":74,"hasResults":11,"nctId":75,"briefTitle":76,"officialTitle":77,"acronym":78,"eligibilityCriteria":79,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":80,"targetDuration":4,"studyType":23,"phases":82,"briefSummary":83,"conditions":84,"keywords":85,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":96,"completionDateStruct":98,"leadSponsor":100,"locationsCount":102},"100646180","injection-site-in-ultrasound-guided-interscalene-block-for-shoulder-arthroscopy-100646180","NCT07695025","Injection Site in Ultrasound-Guided Interscalene Block for Shoulder Arthroscopy","Does the Injection Site of Local Anesthetic Around the C5-C7 Nerve Roots Affect Block Success and Complication Rates During Ultrasound-Guided Interscalene Block for Shoulder Arthroscopy?","ISB-ROOT","Inclusion Criteria:\n\nAdults aged 18 years or older. ASA physical status I-III. Scheduled for shoulder arthroscopy under general anesthesia with a planned ultrasound-guided interscalene block for postoperative analgesia.\n\nAble to provide written informed consent. Normal coagulation parameters and no antithrombotic therapy. No infection or anatomical abnormality at the injection site. No known allergy to local anesthetics. No contralateral diaphragmatic paralysis or pneumothorax. No dyspnea and adequate pulmonary function.\n\nExclusion Criteria:\n\nAge younger than 18 years or ASA physical status IV. Antithrombotic therapy or abnormal coagulation parameters. Infection or anatomical abnormality at the injection site. Known allergy to local anesthetics. Contralateral diaphragmatic paralysis or history of pneumothorax. Dyspnea. Refusal to undergo interscalene block.",{"count":81,"type":22},50,[25],"Ultrasound-guided interscalene block is commonly used for postoperative analgesia in patients undergoing shoulder arthroscopy. The location of local anesthetic injection may influence both block efficacy and the incidence of block-related complications. This randomized, double-blind clinical trial compares two different injection sites around the C5-C7 nerve roots using the same local anesthetic dose and volume. The study will assess block success, postoperative analgesia, opioid consumption, diaphragmatic function, and procedure-related complications.",[29,28],[86,87,88,29,89,90,91,92],"Ultrasound-Guided Interscalene Block","Interscalene Block","Regional Anesthesia","Postoperative Analgesia","Local Anesthetic","Brachial Plexus Block","Phrenic Nerve","2026-07-05",{"date":95,"type":43},"2026-07-10",{"date":97,"type":22},"2026-07-15",{"date":99,"type":22},"2026-11-30",{"name":101,"class":71},"Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey",1,{"id":104,"slug":105,"hasResults":11,"nctId":106,"briefTitle":107,"officialTitle":108,"acronym":109,"eligibilityCriteria":110,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":111,"enrollmentInfo":112,"targetDuration":4,"studyType":23,"phases":114,"briefSummary":115,"conditions":116,"keywords":117,"overallStatus":121,"whyStopped":4,"lastUpdateSubmitDate":122,"lastUpdatePostDateStruct":123,"startDateStruct":125,"completionDateStruct":126,"leadSponsor":128,"locationsCount":102},"100644008","interscalene-brachial-plexus-block-versus-serratus-posterior-superior-intercostal-plane-block-for-arthroscopic-shoulder-surgery-100644008","NCT07668648","Interscalene Brachial Plexus Block Versus Serratus Posterior Superior Intercostal Plane Block for Arthroscopic Shoulder Surgery","Comparison of Interscalene Brachial Plexus Block and Serratus Posterior Superior Intercostal Plane Block for Postoperative Analgesia After Arthroscopic Shoulder Surgery: A Prospective, Randomized, Double-Blind Controlled Trial","SISA","Inclusion Criteria:\n\n* Age between 18 and 75 years\n* ASA physical status I, II, or III\n* Scheduled for elective arthroscopic shoulder surgery under general anesthesia\n* Provision of written informed consent\n\nExclusion Criteria:\n\n* Refusal to participate in the study\n* Coagulopathy\n* Current anticoagulant therapy\n* Infection at the block site\n* Previous surgery involving the planned block site\n* Known allergy or history of toxicity to local anesthetics\n* Hepatic failure\n* Renal failure\n* Uncontrolled diabetes mellitus\n* Cognitive impairment or mental disability preventing reliable assessment\n* Chronic opioid use or ongoing chronic pain treatment\n* Pregnancy, suspected pregnancy, or breastfeeding\n* Chronic pulmonary disease (e.g., COPD or asthma)\n* Failed block","75 Years",{"count":113,"type":22},80,[25],"Arthroscopic shoulder surgery is associated with moderate to severe postoperative pain that may delay recovery and rehabilitation. Interscalene brachial plexus block (ISB) is widely used for postoperative analgesia in shoulder surgery; however, it may be associated with complications such as phrenic nerve paralysis. The serratus posterior superior intercostal plane (SPSIP) block is a recently described fascial plane block that may provide effective analgesia while avoiding some of the limitations of ISB.\n\nThis prospective, randomized, double-blind controlled trial aims to compare the analgesic efficacy of ISB and SPSIP block in patients undergoing elective arthroscopic shoulder surgery under general anesthesia. The primary outcome is total postoperative opioid consumption during the first 24 hours after surgery. Secondary outcomes include postoperative pain scores, quality of recovery, time to first rescue analgesia, rescue analgesic requirements, intraoperative opioid consumption, sensory block distribution, motor block characteristics, and block-related complications.",[28,29],[118,119,88,120],"Interscalene Brachial Plexus Block","Serratus Posterior Superior Intercostal Plane Block","Ultrasound-Guided Nerve Block","RECRUITING","2026-06-25",{"date":124,"type":43},"2026-06-29",{"date":122,"type":43},{"date":127,"type":22},"2026-12-15",{"name":129,"class":50},"Ferit Yetik",{"id":131,"slug":132,"hasResults":11,"nctId":133,"briefTitle":134,"officialTitle":135,"acronym":4,"eligibilityCriteria":136,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":137,"enrollmentInfo":138,"targetDuration":4,"studyType":23,"phases":140,"briefSummary":141,"conditions":142,"keywords":143,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":148,"lastUpdatePostDateStruct":149,"startDateStruct":151,"completionDateStruct":153,"leadSponsor":155,"locationsCount":102},"100621334","continuous-cervical-erector-spinae-plane-block-versus-interscalene-nerve-block-in-shoulder-arthroscopic-surgery-100621334","NCT07369271","Continuous Cervical Erector Spinae Plane Block Versus Interscalene Nerve Block in Shoulder Arthroscopic Surgery","Continuous Cervical Erector Spinae Plane Block Versus Interscalene Nerve Block in Shoulder Arthroscopic Surgery- A Randomized Controlled Trial","Inclusion Criteria:\n\n* Adult patients scheduled for elective shoulder arthroscopic surgery\n\nExclusion Criteria:\n\n* Contraindications to regional analgesia\n* BMI \\>40\n* ASA physical status IV\n* history of drug or opioid abuse\n* preoperative upper limb motor impairment\n* postoperative ventilator support or ICU admission\n* Inability to provide self-reported pain assessments","80 Years",{"count":139,"type":22},165,[25],"Shoulder arthroscopic surgery is associated with moderate to severe postoperative pain, which may hinder early mobilization and functional recovery. Interscalene block (ISB) is commonly used to provide effective analgesia but is frequently associated with hemidiaphragmatic paralysis due to phrenic nerve involvement. Cervical erector spinae plane block (ESPB) has been proposed as an alternative regional technique that may provide analgesia while reducing respiratory-related adverse effects. This randomized controlled trial aims to compare the analgesic efficacy and safety of cervical ESPB versus continuous ISB in patients undergoing shoulder arthroscopic surgery.",[29],[36,144,145,146,147],"postoperative pain","regional anesthesia","interscalene block","erector spinae plane block","2026-01-17",{"date":150,"type":43},"2026-01-27",{"date":152,"type":22},"2026-01-15",{"date":154,"type":22},"2028-01-31",{"name":156,"class":71},"National Cheng-Kung University Hospital",{"id":158,"slug":159,"hasResults":11,"nctId":160,"briefTitle":161,"officialTitle":162,"acronym":4,"eligibilityCriteria":163,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":111,"enrollmentInfo":164,"targetDuration":4,"studyType":166,"phases":4,"briefSummary":167,"conditions":168,"keywords":172,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":174,"lastUpdatePostDateStruct":175,"startDateStruct":176,"completionDateStruct":178,"leadSponsor":180,"locationsCount":102},"100619345","effect-of-anesthesia-technique-on-surgical-view-in-shoulder-arthroscopy-100619345","NCT07343414","Effect of Anesthesia Technique on Surgical View in Shoulder Arthroscopy","Impact of Anesthesia Method on Surgical View and Surgeon Satisfaction During Shoulder Arthroscopy: A Prospective Observational Study","Inclusion Criteria:\n\n* Volunteers aged 18 to 75 years.\n* Patients scheduled for elective shoulder arthroscopy.\n* Patients with an ASA (American Society of Anesthesiologists) physical status score of I, II, or III.\n* Patients capable of providing informed consent.\n\nExclusion Criteria:\n\n* Previous surgical procedure performed on the same shoulder.\n* Presence of medical contraindications that could affect the choice of anesthesia (coagulopathy, active infection, severe pulmonary diseases)\n* Known allergy to local anesthetics or general anesthesia agents\n* History of opioid dependence or chronic pain syndrome\n* Presence of neurological disorders, particularly those involving the brachial plexus",{"count":165,"type":22},82,"OBSERVATIONAL","This prospective observational study evaluates the effect of the anesthesia method (general anesthesia versus regional anesthesia \\[interscalene nerve block\u002Fsuperficial cervical block\\] with sedation) on the operating clarity of the surgical view and the surgeon's satisfaction during elective shoulder arthroscopy. The study investigates how these different anesthesia techniques influence intraoperative conditions, specifically bleeding amounts and the visibility of the surgical field, which are critical for the success of this minimally invasive procedure. Additionally, the research will monitor patient-centered outcomes, including postoperative pain levels, recovery time, and potential side effects such as nausea or vomiting, to determine which anesthesia strategy provides the optimal balance of surgical efficiency and patient comfort.",[29,169,170,171],"Interscalene Nerve Block","Surgical View Quality","Surgeon Satisfaction",[29,171,170,169,173],"Rotator Cuff Repair","2026-01-07",{"date":152,"type":43},{"date":177,"type":22},"2026-02-01",{"date":179,"type":22},"2027-05-01",{"name":181,"class":71},"Amasya University",{"id":183,"slug":184,"hasResults":11,"nctId":185,"briefTitle":186,"officialTitle":186,"acronym":4,"eligibilityCriteria":187,"healthyVolunteers":188,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":189,"targetDuration":4,"studyType":166,"phases":4,"briefSummary":191,"conditions":192,"keywords":4,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":193,"lastUpdatePostDateStruct":194,"startDateStruct":196,"completionDateStruct":198,"leadSponsor":200,"locationsCount":102},"100558589","development-of-the-surgeon-satisfaction-self-assessment-questionnaire-for-shoulder-arthroscopy-100558589","NCT06553079","Development of the Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy","Inclusion Criteria:\n\n* Orthopedic Surgeons:Must be a licensed orthopedic surgeon actively performing shoulder arthroscopy procedures.\n* Participants must be willing to provide informed consent and participate in both the questionnaire development (including interviews) and the validation phases of the study.\n* Participants must be proficient in the language in which the questionnaire is administered to ensure accurate and meaningful responses.\n\nExclusion Criteria:\n\n\\-",true,{"count":190,"type":22},30,"This observational study aims to develop and validate the \"Surgeon Satisfaction Self-Assessment Questionnaire for Shoulder Arthroscopy.\" The study involves conducting in-depth interviews with surgeons who perform shoulder arthroscopy to identify key factors influencing their surgical satisfaction, including individual, patient-related, and surgical equipment-related factors. Based on the insights gained from these interviews, a comprehensive questionnaire will be developed. The questionnaire will then undergo validation processes, including assessments of content, construct, criterion, and reliability, to ensure it accurately and consistently measures surgeon satisfaction. The final validated tool is intended to provide a reliable method for surgeons to self-assess their satisfaction with shoulder arthroscopy procedures, contributing to improved surgical practices and outcomes.",[171,29],"2024-08-10",{"date":195,"type":43},"2024-08-14",{"date":197,"type":22},"2024-09-01",{"date":199,"type":22},"2025-03-01",{"name":201,"class":71},"Gazi University"]