[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100596527":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":34,"locations":25,"responsibleParty":42,"collaborators":25,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":25,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":53,"minAge":54,"maxAge":25,"enrollmentInfo":55,"targetDuration":25,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":25,"overallStatus":67,"whyStopped":25,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":72,"completionDateStruct":74,"leadSponsor":76,"locationsCount":25},{"fullName":5,"class":6},"Ordu University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Control Group","ACTIVE_COMPARATOR","Group where no intervention will be applied",[13],"Behavioral: Infusion monitoring system developed for use by nurses in patient care",{"label":15,"type":16,"description":17,"interventionNames":18},"Experimental group","EXPERIMENTAL","The group to which the intervention will be applied",[13],[20],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"BEHAVIORAL","Infusion monitoring system developed for use by nurses in patient care","In the experimental group, the frequency of complications will first be determined and an infusion monitoring system will be developed and used by nurses in patient care.",[9,15],null,[27,30],{"name":28,"affiliation":5,"role":29},"Fatma Aksoy, MscN","PRINCIPAL_INVESTIGATOR",{"name":31,"affiliation":32,"role":33},"Şule Bıyık Bayram, PhD","Karadeniz Technical University","STUDY_DIRECTOR",[35,40],{"name":36,"role":37,"phone":38,"phoneExt":25,"email":39},"Fatma Aksoy, MScN","CONTACT","+905389529328","fatma.aksoyy96@gmail.com",{"name":31,"role":37,"phone":25,"phoneExt":25,"email":41},"sulebiyik@gmail.com",{"type":29,"investigatorFullName":43,"investigatorTitle":44,"investigatorAffiliation":5,"oldNameTitle":25,"oldOrganization":25},"Fatma Aksoy","Principal Investigator","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":56,"type":57},102,"ESTIMATED","INTERVENTIONAL",[60],"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%.",[63,64,65,66],"Extravasation","Intensive Care Units (ICUs)","Phlebitis","Infiltration","NOT_YET_RECRUITING","2025-11-14",{"date":70,"type":71},"2025-11-17","ACTUAL",{"date":73,"type":57},"2025-11-08",{"date":75,"type":57},"2026-07-08",{"name":5,"class":6}]