[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Adiyaman University\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":199},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,46,78,105,132,154,174],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100650735","fresh-gas-flow-and-lung-ultrasonography-in-laparoscopic-cholecystectomy-100650735",false,"NCT07753278","Fresh Gas Flow and Lung Ultrasonography in Laparoscopic Cholecystectomy","Evaluation of the Effects of Fresh Gas Flow Differences on the Lungs Using Ultrasonography in Laparoscopic Cholecystectomy Surgeries","Inclusion Criteria:\n\n* Adults aged 18 years or older.\n* American Society of Anesthesiologists (ASA) physical status I-II.\n* Scheduled for elective laparoscopic cholecystectomy under general anesthesia.\n* Able and willing to provide written informed consent.\n\nExclusion Criteria:\n\n* Refusal to participate in the study.\n* History of chronic respiratory disease, including severe asthma, chronic obstructive pulmonary disease (COPD), or bronchiolitis.\n* History of alcohol or substance abuse.\n* Intraoperative airway or respiratory complications during endotracheal intubation or surgery.\n* Life-threatening postoperative complications.\n* Patients with ASA physical status III or higher.","ALL","18 Years","65 Years",{"count":20,"type":21},120,"ESTIMATED","INTERVENTIONAL",[24],"NA","This prospective randomized clinical trial aims to evaluate the effects of different fresh gas flow rates on postoperative pulmonary aeration using lung ultrasonography in patients undergoing elective laparoscopic cholecystectomy. Patients will be randomly assigned to receive either low-flow anesthesia (0.5 L\u002Fmin) or high-flow anesthesia (4 L\u002Fmin) during maintenance of general anesthesia. The primary objective is to compare postoperative lung ultrasound scores and the incidence of atelectasis between the two groups.",[27,28],"Postoperative Atelectasis","Pulmonary Atelectasis",[30,31,32],"Fresh Gas Flow","Lung Ultrasound Score","Pulmonary Complications","NOT_YET_RECRUITING","2026-08-04",{"date":36,"type":37},"2026-08-07","ACTUAL",{"date":39,"type":21},"2026-08-15",{"date":41,"type":21},"2026-10-15",{"name":43,"class":44},"Adiyaman University","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":51,"acronym":52,"eligibilityCriteria":53,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":54,"enrollmentInfo":55,"targetDuration":4,"studyType":22,"phases":57,"briefSummary":58,"conditions":59,"keywords":65,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":45},"100646601","vr-effects-after-hip-replacement-surgery-pain-100646601","NCT07689461","VR Effects After Hip Replacement Surgery Pain","The Effect of Virtual Reality on Pain, Anxiety, and Comfort Levels After Total Hip Replacement Surgery","THA","Inclusion Criteria:\n\n* Patients scheduled for elective surgery who agree to participate in the study,\n* Individuals 18 years of age or older,\n* Those with adequate cognitive function,\n* Those who have not previously undergone total hip replacement surgery,\n* Those who volunteer to participate in the study and sign the informed consent form,\n* Patients with a pain score (on a scale of 1 to 10) of 4 or higher were included in the study.\n\nExclusion Criteria:\n\n* Individuals under the age of 18,\n* Those previously diagnosed with a chronic pain syndrome (other than hip osteoarthritis),\n* Individuals with impaired cognitive function (severe psychiatric disorders),\n* Individuals who have previously undergone total hip replacement surgery,\n* Individuals with severe hearing or visual impairments,\n* Individuals with a history of opioid dependence,\n* Patients with a pain score (on a scale of 1 to 10) of 4 or lower were excluded from the study.","99 Years",{"count":56,"type":21},80,[24],"Total Hip Arthroplasty (THA), a procedure performed to enhance the quality of life, is accompanied by postoperative challenges such as pain and anxiety that adversely affect patient comfort. Inadequate management of these complications can prolong the length of hospital stay, delay recovery, lead to functional impairments, and elevate the risk of chronic pain development. Conventional pharmacological interventions employed for management are limited due to their potential for adverse effects and dependency. Virtual reality (VR) is a non-pharmacological distraction technique utilized in the healthcare sector, leveraging advanced technology to maximize patient comfort by alleviating pain and minimizing anxiety.\n\nA review of the literature reveals that while the use of VR has positive effects on pain and anxiety, there is a notable scarcity of high-quality randomized controlled trials concurrently evaluating its impact on pain, anxiety, and comfort levels in postoperative orthopedic procedures such as THA. In this randomized controlled trial, participants in the control group will receive standard care, whereas those in the experimental group will receive a 30-minute VR intervention-offering three distinct options-in addition to standard care during the acute phase of the first 48 hours. Postoperative assessments will be conducted using the Visual Analogue Scale (VAS) for pain intensity, the State Anxiety Inventory for anxiety levels, and the Perianesthesia Comfort Scale for comfort levels.\n\nBy evaluating the potential of VR as a non-pharmacological adjuvant in post-THA care, the findings of this study will provide significant contributions to evidence-based nursing practices aimed at developing multimodal pain management strategies, reducing opioid consumption, and enhancing patient satisfaction.",[60,61,62,63,64],"Virtual Reality","Hip Arthropathy","Comfort","Anxiety","Pain, Postoperative",[60,66,67,63,68],"Total Hip Arthroplasty","Postoperative Pain","Comfort Level","RECRUITING","2026-07-01",{"date":72,"type":37},"2026-07-08",{"date":74,"type":37},"2025-10-21",{"date":76,"type":21},"2026-12-31",{"name":43,"class":44},{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":4,"eligibilityCriteria":84,"healthyVolunteers":11,"sex":85,"minAge":86,"maxAge":17,"enrollmentInfo":87,"targetDuration":4,"studyType":22,"phases":89,"briefSummary":90,"conditions":91,"keywords":95,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":45},"100577086","technological-devices-in-circumcision-100577086","NCT06793722","Technological Devices in Circumcision","The Effect of Technological Devices on the Child's Pain and Anxiety Level in Circumcision Performed With Local Anesthesia","Inclusion Criteria:\n\n* Circumcision for medical or religious reasons.\n\nExclusion Criteria:\n\n* Children with chronic diseases.\n* Children with genital medical problems.\n* Children with mental and communication disabilities and their parents.","MALE","6 Years",{"count":88,"type":21},50,[24],"It aims to investigate the effect of circumcision on the pain and anxiety level of children who are circumcised by watching videos\u002Fplaying games during the procedure. Previous studies have been conducted to explain the procedure with informative videos and games before circumcision, and reductions in anxiety and pain levels have been detected. The research will start with hospitalization and end with a check-up after discharge.",[92,93,94],"Circumcision Adult","Circumcision, Male","Circumcision",[96],"circumcision","2025-09-29",{"date":99,"type":37},"2025-10-02",{"date":101,"type":37},"2025-01-20",{"date":103,"type":21},"2025-12-31",{"name":43,"class":44},{"id":106,"slug":107,"hasResults":11,"nctId":108,"briefTitle":109,"officialTitle":110,"acronym":4,"eligibilityCriteria":111,"healthyVolunteers":112,"sex":113,"minAge":17,"maxAge":114,"enrollmentInfo":115,"targetDuration":4,"studyType":22,"phases":116,"briefSummary":117,"conditions":118,"keywords":120,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":125,"lastUpdatePostDateStruct":126,"startDateStruct":128,"completionDateStruct":130,"leadSponsor":131,"locationsCount":45},"100607105","effect-of-motivational-counseling-on-the-intention-to-use-modern-contraceptive-methods-100607105","NCT07184229","Effect of Motivational Counseling on the Intention to Use Modern Contraceptive Methods","Motivational Interviewing-Based Family Planning Counseling and Its Effect on Attitudes and Intentions Toward Modern Contraceptive Use Among Women Using Traditional Contraceptive Methods","Inclusion Criteria:\n\nWomen aged between 18 and 49 years\n\n* Literate in Turkish\n* Currently using a traditional family planning method (e.g., withdrawal method)\n\nExclusion Criteria:\n\n* Diagnosed psychiatric disorder\n* Currently pregnant",true,"FEMALE","49 Years",{"count":20,"type":21},[24],"This study aims to evaluate the effect of motivational interviewing-based family planning counseling on attitudes and intentions toward modern contraceptive methods among women currently using traditional contraceptive methods. Despite the widespread use of traditional methods in many regions, including Turkey, modern contraceptive methods remain underutilized, leading to increased unintended pregnancies and related health burdens. Motivational interviewing is a client-centered counseling approach that supports individuals in making informed health decisions. By providing tailored counseling, this study seeks to improve women's awareness and motivation to adopt effective modern contraceptive methods, ultimately enhancing reproductive health outcomes. The findings are expected to contribute valuable insights for healthcare providers to improve family planning services and support women's reproductive choices.",[119],"Contraception",[121,122,123,124],"traditional contraceptive methods","family planning","motivational interviewing","women","2025-09-20",{"date":127,"type":37},"2025-09-25",{"date":129,"type":21},"2025-09-16",{"date":103,"type":21},{"name":43,"class":44},{"id":133,"slug":134,"hasResults":11,"nctId":135,"briefTitle":136,"officialTitle":137,"acronym":4,"eligibilityCriteria":138,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":139,"targetDuration":4,"studyType":22,"phases":141,"briefSummary":142,"conditions":143,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":146,"lastUpdatePostDateStruct":147,"startDateStruct":149,"completionDateStruct":151,"leadSponsor":153,"locationsCount":45},"100577374","three-dimensional-virtual-reconstruction-3d-in-percutaneous-nephrolithotomy-100577374","NCT06797466","Three Dimensional Virtual Reconstruction (3D) in Percutaneous Nephrolithotomy","Investigation of the Effect of Three Dimensional Virtual Reconstruction (3D) on Percutaneous Nephrolithotomy Learning Curve in Specialist Training","Inclusion Criteria:\n\n* Patients with kidney stones larger than 2 cm and those with PCNL indication.\n\nExclusion Criteria:\n\n* Patients with missing CT images, missing clinical information, or inaccessible",{"count":140,"type":21},100,[24],"The aim of our study is to investigate the effect of 3D imaging technique on the PCNL learning curve in specialist training.",[144,145],"PNL","Stone, Kidney","2025-05-08",{"date":148,"type":37},"2025-05-09",{"date":150,"type":37},"2025-01-21",{"date":152,"type":21},"2025-10-31",{"name":43,"class":44},{"id":155,"slug":156,"hasResults":11,"nctId":157,"briefTitle":158,"officialTitle":159,"acronym":4,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":161,"targetDuration":4,"studyType":22,"phases":163,"briefSummary":164,"conditions":165,"keywords":4,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":171,"leadSponsor":173,"locationsCount":45},"100577204","homework-in-retrograde-intrarenal-surgery-100577204","NCT06795256","Homework in Retrograde Intrarenal Surgery","Homework to Help with Stone Dissolution in Retrograde Intrarenal Surgery","Inclusion Criteria:\n\n* Patients with an indication for RIRC\n\nExclusion Criteria:\n\n* Patients with anatomic abnormalities such as horseshoe kidney, fragments in the calyx diverticulum, infundibular stenosis, pelvi-ureteral junction obstruction or ureteral stenosis.\n* Patients with morbid obesity, uncontrolled hypertension, previous cerebrovascular accident, skeletal deformity such as significant coronary artery disease or symptomatic gastro-esophageal reflux disease.\n* Patients with lumbar disc herniation who have undergone spinal surgery and are unable to undergo behavioral therapy.",{"count":162,"type":21},200,[24],"To evaluate the effectiveness of this homework on stone clearance rates after retrograde intrarenal surgery (RIRS) by instructing the patient in the home environment and suggesting percussion and movement\u002Fposition changes to assist in spontaneous stone passage.",[166,145],"Retrograde Intrarenal Surgery","2025-01-27",{"date":169,"type":37},"2025-01-29",{"date":150,"type":37},{"date":172,"type":21},"2025-11-30",{"name":43,"class":44},{"id":175,"slug":176,"hasResults":11,"nctId":177,"briefTitle":178,"officialTitle":179,"acronym":4,"eligibilityCriteria":180,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":181,"targetDuration":4,"studyType":22,"phases":183,"briefSummary":184,"conditions":185,"keywords":187,"overallStatus":69,"whyStopped":4,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":192,"startDateStruct":194,"completionDateStruct":196,"leadSponsor":198,"locationsCount":45},"100546294","gram-stain-of-the-first-urine-after-puncture-in-percutaneous-nephrolithotomy-100546294","NCT06393062","Gram Stain of the First Urine After Puncture in Percutaneous Nephrolithotomy","Gram Stain of the First Urine After Intraoperative Renal Puncture in Predicting the Systemic Inflammatory Response After Percutaneous Nephrolithotomy: A Prospective, Randomized Controlled Study","Inclusion Criteria:\n\n* patients with an indication for percutaneous nephrolithotomy due to kidney stone disease.\n\nExclusion Criteria:\n\n* under 18 years old,\n* having an active urinary tract infection before surgery and positive urine cultures,\n* Patients with bilateral kidney stones,\n* DJ stent or nephrostomy placement,\n* Solitary kidney stones,\n* Bleeding disorders,\n* impaired kidney function,\n* a history of antibiotic use for any reason within 2 weeks before randomization were excluded from the study.",{"count":182,"type":21},245,[24],"In this study, investigators compared the systemic inflammatory responses after percutaneous nephrolithotomy (PCNL) patients who were given an expanded empirical antibiotic regimen based on the prediction of the possibility of bacteria identified by Gram staining the first urine after renal puncture and patients whose antibiotic regimen was not performed and whose antibiotic regimen was adjusted according to patient symptoms and culture results. Investigators aimed to test its diagnostic value in predicting and preventing complications.",[186],"Percutaneous Nephrolithotomy",[188,189,190,191],"fever","gram stain","percutaneous nephrolithotomy","Systemic inflammatory response syndrome (SIRS)",{"date":193,"type":37},"2025-01-22",{"date":195,"type":37},"2022-12-01",{"date":197,"type":21},"2025-09-30",{"name":43,"class":44},""]