[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"infiltration\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:infiltration":30},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,43,71],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":31,"whyStopped":4,"lastUpdateSubmitDate":32,"lastUpdatePostDateStruct":33,"startDateStruct":36,"completionDateStruct":38,"leadSponsor":40,"locationsCount":4},"100596527","prevention-of-phlebitis-infiltration-and-extravasation-with-infusion-monitoring-system-100596527",false,"NCT07046624","Prevention of Phlebitis, Infiltration and Extravasation With Infusion Monitoring System","Development of an Infusion Monitoring System to Prevent Phlebitis, Infiltration and Extravasation and Its Application in the Intensive Care Unit","Inclusion Criteria:\n\n* 18 years of age and older\n* Receiving medication via peripheral intravenous catheter,\n* Monitored daily for signs of phlebitis, infiltration and extravasation,\n* Patients who can speak\n\nExclusion Criteria:\n\n* Unconscious patients",true,"ALL","18 Years",{"count":20,"type":21},102,"ESTIMATED","INTERVENTIONAL",[24],"NA","Peripheral venous catheter complications are conditions that are frequently seen in intensive care clinics and require nursing care. The most common complications are phlebitis, infiltration and extravasation. Nurses should take the necessary precautions to prevent these complications from developing.. Therefore, this planned thesis study aims to establish an infusion monitoring system and evaluate its effectiveness in early detection of complications related to peripheral intravenous catheters. The research is planned as a randomized controlled experimental study. The study will be conducted in Ordu State Hospital General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The universe of the study will consist of patients receiving inpatient treatment in General Intensive Care Unit 1 and General Intensive Care Unit 3 clinics. The sample size will be determined by g-power analysis after a two-month preliminary follow-up. Data will be collected with the \"Clinical Follow-up Form\", \"Patient Information Form\", and \"Complication Follow-up Form\". The clinics included in the study will be divided into two groups as experimental and control groups. First, the frequency of complications will be determined in the experimental and control groups. Then, while the control group continues its routine protocol and applications, an infusion follow-up system will be developed in the experimental group and will be used by nurses in patient care. In the final stage, the frequency of peripheral venous catheter complications will be determined again. Data will be evaluated using the SPSS 22.0 package program at a significance level of p\\\u003C0.05 and a confidence interval of 95%.",[27,28,29,30],"Extravasation","Intensive Care Units (ICUs)","Phlebitis","Infiltration","NOT_YET_RECRUITING","2025-11-14",{"date":34,"type":35},"2025-11-17","ACTUAL",{"date":37,"type":21},"2025-11-08",{"date":39,"type":21},"2026-07-08",{"name":41,"class":42},"Ordu University","OTHER",{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":51,"targetDuration":53,"studyType":54,"phases":4,"briefSummary":55,"conditions":56,"keywords":57,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":61,"lastUpdatePostDateStruct":62,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":70},"100600869","infiltration-in-rheumatology-with-3d-virtual-reality-headset-pilot-study-for-the-evaluation-of-satisfaction-icare-100600869","NCT07103096","Infiltration in Rheumatology With 3D Virtual Reality Headset Pilot Study for the Evaluation of Satisfaction (ICARE)","Infiltration in Rheumatology With 3D Virtual Reality Headset Pilot Study for the Evaluation of Satisfaction and Feasibility According to Location (Icare)","Icare","Inclusion Criteria:\n\n* 18 years or older\n* Patient requiring infiltration of the spine (high epidural or sacrococcygeal hiatus) of the subacromial-deltoid bursa or the knee, regardless of the product infiltrated\n* Within the Rheumatology department of Saint-Antoine hospital (consultation or hospitalized)\n\nExclusion Criteria:\n\n* History of severe psychiatric disorders - History of epilepsy\n* Cognitive disorders\n* Language barrier - Hearing aid-assisted deafness and\u002For ophthalmological problems leading to a major loss of vision (advanced cataract, visual impairment)\n* Infiltration of the spine (high epidural or sacrococcygeal hiatus), subacromial-deltoid bursa or knee \\\u003C 6 months\n* Characterized depressive disorder diagnosed recently (for less than 6 months) or not stabilized\n* Previous use of a virtual reality headset during treatment\n* Being under guardianship or curatorship",{"count":52,"type":21},30,"1 Day","OBSERVATIONAL","This study is to evaluate the satisfaction and feasibility according to the location of the use of a 3D virtual reality headset during an infiltration in rheumatology.",[30],[58,59],"infiltration","3D virtual reality headset","RECRUITING","2025-07-28",{"date":63,"type":35},"2025-08-05",{"date":65,"type":35},"2025-05-28",{"date":67,"type":21},"2026-05",{"name":69,"class":42},"Assistance Publique - Hôpitaux de Paris",1,{"id":72,"slug":73,"hasResults":11,"nctId":74,"briefTitle":75,"officialTitle":76,"acronym":4,"eligibilityCriteria":77,"healthyVolunteers":11,"sex":17,"minAge":78,"maxAge":4,"enrollmentInfo":79,"targetDuration":4,"studyType":22,"phases":81,"briefSummary":82,"conditions":83,"keywords":85,"overallStatus":60,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":70},"100470607","comparison-of-the-analgesic-effect-of-2-shoulder-infiltrations-100470607","NCT05408065","Comparison of the Analgesic Effect of 2 Shoulder Infiltrations","A Randomized Single-blinded Clinical Trial of the Efficacy of Intra-articular Infiltration of Cingal (Sodium Hyaluronate\u002FTriamcinolone) Versus Cortisone (Triamcinolone) in Patients With Osteoarthritis of the Shoulder.","Inclusion Criteria:\n\n* A clinical examination that confirms the radiological diagnosis of moderate to severe primary shoulder osteoarthritis, stage II and above, according to the Samilson-Prieto classification.\n* Patients aged between 20 and 90 years.\n* A patient with bilateral shoulder osteoarthritis will choose the side of the infiltration, only one side can be chosen to participate in the study.\n* The patient must have a clinical pain threshold of a minimum of 4\u002F10 on the visual analogue scale.\n* The patient must have the cognitive ability to read and fill out the questionnaires.\n* The patient must be able to read and understand French or English\n\nExclusion Criteria:\n\n* Presence of a transfixing rotator cuff tear assessed on MRI.\n* No previous shoulder reconstruction surgery.\n* Pregnant woman.\n* A patient who has received a cortisone infiltration within 6 months prior to the start of the study.\n* A patient who has received a platelet-rich plasma or a hyaluronic acid infiltration within 12 months prior to the start of the study.\n* Diagnosis of avascular necrosis.\n* Disease affecting the studied joint (systemic inflammatory disease, history of septic arthritis, osteonecrosis, etc.)\n* Suspicion or presence of active local infectious process.\n* Presence or suspicion of neoplasia or local metastasis.\n* Severe trauma to the shoulder ( ≤ 3 months)\n* Significant cognitive impairment or insufficient language proficiency to adequately answer the questionnaires.\n* Any other serious medical condition that does not allow participation in the study or may be a contraindication to cortisone injection.","20 Years",{"count":80,"type":21},84,[24],"For patients suffering of osteoarthritis, only analgesic treatments such as anti-inflammatory drugs and cortisone infiltrations provide significant but temporary relief of their pain. The objective is to compare the analgesic effect of 2 infiltrations: Cingal (sodium hyaluronate and triamcinolone) versus cortisone (triamcinolone). It is anticipated that the Cingal infiltration will have a greater analgesic effect than a simple cortisone infiltration in patients with moderate to severe osteoarthritis of the shoulder.\n\nMethod:\n\n* Randomized controlled trial\n* Monocentric\n* Randomization will be done using sealed envelopes",[30,84],"Shoulder Osteoarthritis",[58,86,87],"Osteoarthritis","hyaluronic acid","2024-02-09",{"date":90,"type":35},"2024-02-12",{"date":92,"type":35},"2022-11-15",{"date":94,"type":21},"2026-12",{"name":96,"class":42},"Centre hospitalier de l'Université de Montréal (CHUM)"]