[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"upper-limb-injury\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:upper-limb-injury":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,44,69],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":4,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":43},"100568735","translation-and-validation-of-the-limbs-pain-autonomy-depression-anxiety-and-quality-of-life-scales-in-albanian-100568735",false,"NCT06685094","Translation and Validation of the Limbs, Pain, Autonomy, Depression, Anxiety and Quality of Life Scales in Albanian","Cross-cultural Adaptation, Translation and Validation of the Assessment Scales of the Upper and Lower Limbs, Pain, Autonomy, Depression, Anxiety and Quality of Life for Use in the Albanian-speaking Population","Inclusion Criteria:\n\n* articular and muscular pain\n* back pain\n* presence of rheumatologic symptoms\n* functional misbalance\n* scoliosis\n* musculoskeletal disorders\n\nExclusion Criteria:\n\n* no native albanian language\n* severe trauma to the lumbar spine or hip(s)\n* tumor\n* metabolic disease",true,"ALL","18 Years","80 Years",{"count":21,"type":22},300,"ESTIMATED","OBSERVATIONAL","The cross-cultural adaptation will be performed according to the internationally recommended methodology, using the following guidelines: translation, back-translation; revision by a committee, questionnaire diffusion and data collection and analyzing.\n\nThe psychometric properties will be evaluated by administering the questionnaire to approximately 300 participants. Reliability will be estimated through stability and homogeneity assessment",[26,27,28,29,30],"Musculoskeletal Pain","Autonomy","Healthy","Upper Limb Injury","Lower Limb Injury","RECRUITING","2026-06-02",{"date":34,"type":35},"2026-06-04","ACTUAL",{"date":37,"type":35},"2025-06-30",{"date":39,"type":22},"2027-09-01",{"name":41,"class":42},"Universidad Católica San Antonio de Murcia","OTHER",1,{"id":45,"slug":46,"hasResults":11,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":4,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":51,"enrollmentInfo":52,"targetDuration":4,"studyType":54,"phases":55,"briefSummary":57,"conditions":58,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":4},"100509912","effectiveness-of-images-in-reducing-preoperative-anxiety-100509912","NCT05919602","Effectiveness of Images in Reducing Preoperative Anxiety","Effectiveness of Image Visualization in Reducing Preoperative Anxiety. Pilot Study","Inclusion Criteria:\n\n* Individuals of both sexes over 18 years of age with upper limb pathology that will be surgically treated at the University hospital complex in Salamanca.\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Pathology to be surgically treated with a location other than the upper limb.\n* Patients with a score of less than 26 points on the Mini Mental Examination (MMSE).\n* Blind or visually impaired individuals who cannot correct their vision with appropriate lenses.\n* Any other circumstance at the discretion of the investigators","99 Years",{"count":53,"type":22},167,"INTERVENTIONAL",[56],"NA","Introduction: Current evidence supports the existence of preoperative anxiety and its undesirable effects during surgery and in the postoperative period. Despite numerous studies that have evaluated the effectiveness of different non-pharmacological interventions in reducing preoperative anxiety, we have not found any that use an image catalog.\n\nObjective: To evaluate the effect of an intervention based on the visualization of an image catalog on the improvement of perceived anxiety in patients undergoing upper limb orthopedic surgery.\n\nMethodology: A prospective, randomized, controlled, parallel-group clinical trial with a 1:1 ratio will be conducted. The study will include 167 patients scheduled for upper limb surgery who are over 18 years old, without blindness or decreased visual acuity that cannot be corrected with appropriate lenses. The subjects will be invited to explain the study's objective and perform baseline assessments. On the day of the surgical intervention, both groups will receive standard care, but those in the intervention group will also visualize a catalog of 8 images, 25 minutes before entering the operating room. In addition, 30 and 10 minutes before the intervention begins, all patients included in the study will have vital signs taken, be administered Spielberger's anxiety scale, visual analog scale for anxiety, and cortisol levels in saliva will be determined as measures of preoperative anxiety. The final evaluation will measure whether this intervention results in decreased anxiety, postoperative complications resulting from anxiety, and length of hospital stay.",[29],"NOT_YET_RECRUITING","2025-03-21",{"date":62,"type":35},"2025-03-25",{"date":64,"type":22},"2026-03-01",{"date":66,"type":22},"2027-05-01",{"name":68,"class":42},"María del Mar Perez Saavedra",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":17,"minAge":76,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":54,"phases":79,"briefSummary":80,"conditions":81,"keywords":4,"overallStatus":59,"whyStopped":4,"lastUpdateSubmitDate":82,"lastUpdatePostDateStruct":83,"startDateStruct":85,"completionDateStruct":87,"leadSponsor":89,"locationsCount":43},"100576004","efficacy-and-safety-of-liposomal-bupivacaine-and-ropivacaine-in-upper-limb-surgery-100576004","NCT06779643","Efficacy and Safety of Liposomal Bupivacaine and Ropivacaine in Upper Limb Surgery","Efficacy and Safety of Liposomal Bupivacaine and Ropivacaine in Upper Limb Surgery: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Age: Two years or older.\n* ASA Physical Status: American Society of Anesthesiologists (ASA) physical status classification of I, II, or III.\n* Surgical Indication: Patients requiring surgical treatment for any of the following upper limb injuries: Burn injuries. Digital replantation. Upper limb fractures, including fractures of the radius, ulna, humerus, and carpal bones. Hand fractures, including fractures of the phalanges and metacarpals.\n* Patients scheduled to undergo either a continuous brachial plexus block combined with general anesthesia or general anesthesia alone.\n* Patients (or their legal guardians) provided voluntary written informed consent.\n\nExclusion Criteria:\n\n* Known allergy to local anesthetic agents.\n* Presence of infection or skin disease at the planned puncture site.\n* Severe coagulation disorders or current use of anticoagulant medications that cannot be safely discontinued for the procedure.\n* Presence of severe cardiopulmonary or neurological disease.\n* Inability to cooperate with regional or general anesthesia.\n* Pregnancy or lactation.\n* Presence of severe psychiatric illness or cognitive impairment that would hinder participation.\n* Long-term use of analgesic medications.","2 Years",{"count":78,"type":22},60,[56],"This clinical trial aims to evaluate the efficacy and safety of liposomal bupivacaine and ropivacaine when used in different brachial plexus blocks and epidural anesthesia for the management of pain associated with burn injuries, digital replantation, and upper limb fractures (including radial, ulnar, humeral, and carpal fractures), as well as hand fractures (including phalangeal and metacarpal fractures). The primary objective is to determine whether liposomal bupivacaine or ropivacaine reduces the required postoperative analgesic dosage in these patient populations.\n\nSpecifically, this study will compare brachial plexus blockade with either liposomal bupivacaine or ropivacaine, combined with general anesthesia, against general anesthesia alone to assess the effectiveness of these two local anesthetics in achieving postoperative analgesia.\n\nEnrolled participants will be randomized to one of two treatment arms: either brachial plexus block followed by endotracheal intubation and general anesthesia or general anesthesia alone. Postoperative vital signs, analgesic requirements, and recovery parameters will be continuously monitored and recorded.",[29],"2025-01-13",{"date":84,"type":35},"2025-01-16",{"date":86,"type":22},"2025-02-01",{"date":88,"type":22},"2025-05-10",{"name":90,"class":42},"Xiaguang Duan"]