[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100613943":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":18,"centralContacts":23,"locations":32,"responsibleParty":44,"collaborators":18,"id":48,"slug":49,"hasResults":50,"nctId":51,"briefTitle":52,"officialTitle":53,"acronym":18,"eligibilityCriteria":54,"healthyVolunteers":50,"sex":55,"minAge":56,"maxAge":18,"enrollmentInfo":57,"targetDuration":18,"studyType":60,"phases":61,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":76,"whyStopped":18,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"TC Erciyes University","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Cold Vapor","EXPERIMENTAL","Immediately following the initial (T0) assessment of patients, in addition to routine care and treatment procedures, patients will receive cold vapor using the Hikoneb 906 S\u002FLCD ultrasonic hospital-grade nebulizer device for 15 minutes. Following completion of the intervention, patients' status will be reassessed at 15 (T1) and 30 (T2) minutes.",[13],"Other: Cold Vapor",{"label":15,"type":16,"description":17,"interventionNames":18},"Control Group","NO_INTERVENTION","Patients in the control group will not be subjected to any additional intervention. Follow-up of patients in this group will be conducted in accordance with the clinic's current standard postoperative treatment and care practices, and patients will be evaluated at baseline (T0), 15 minutes (T1), and 30 minutes.",null,[20],{"type":6,"name":9,"description":21,"armGroupLabels":22,"otherNames":18},"Cold steam application will be performed using a Hikoneb 906 S\u002FLCD ultrasonic nebulizer, which will generate cold steam with distilled water. Device parameters will be optimally set to steam delivery level 5 (1-10), steam density level 5 (1-10), and steam temperature 1C0 (1C0-10C0). This application will be applied to the intervention group for 15 minutes after the baseline (T0) assessment. Cold steam will not be delivered directly to the airways but will be applied to the facial area, covering the mouth and nose area. A distance of approximately 20-30 cm will be maintained between the device's steam outlet and the patient's face.",[9],[24,29],{"name":25,"role":26,"phone":27,"phoneExt":18,"email":28},"Yeliz SÜRME, Assoc. Prof. Dr.","CONTACT","+90","yelizsurme@erciyes.edu.tr",{"name":30,"role":26,"phone":27,"phoneExt":18,"email":31},"Ramazan SAKARYA","rs5800s.k.r.y@gmail.com",[33],{"facility":34,"status":18,"city":35,"state":35,"zip":36,"country":37,"countryCode":18,"cosmosGeoPoint":38,"geoPoint":43,"contacts":18},"Erciyes University","Kayseri","38080","Turkey (Türkiye)",{"type":39,"coordinates":40},"Point",[41,42],35.48528,38.73222,{"lat":42,"lon":41},{"type":45,"investigatorFullName":46,"investigatorTitle":47,"investigatorAffiliation":5,"oldNameTitle":18,"oldOrganization":18},"PRINCIPAL_INVESTIGATOR","Yeliz Sürme","Assoc. Prof. Dr.","100613943","the-effect-of-cold-vapor-on-dyspnea-thirst-nausea-and-physiological-parameters-in-the-pacu-after-laparoscopic-inguinal-hernia-surgery-100613943",false,"NCT07273162","The Effect of Cold Vapor on Dyspnea, Thirst, Nausea, and Physiological Parameters in the PACU After Laparoscopic Inguinal Hernia Surgery","The Effect of Cold Vapor Inhalation on Dyspnea Thirst Nausea and Physiological Parameters in the Recovery Unit After Laparoscopic Inguinal Hernia Surgery","Inclusion Criteria:\n\n* Volunteering to participate in the study\n* Being aged 18 years or older\n* Being able to speak and understand Turkish\n* Having cognitive, affective, and communicative competence\n* Having intact visual and auditory functions\n* Having undergone elective laparoscopic inguinal hernia surgery under general anesthesia\n* Having an ASA score of I or II\n* Having a total Modified Aldrete Score of ≥9 and a consciousness score of 2 (fully awake) in the postoperative period\n* Not having developed vomiting prior to the intervention\n* Having a body temperature within the normal physiological range (36-37.5 °C)\n\nExclusion Criteria:\n\n* Having cold vapor application planned by physician order in the PACU prior to the study\n* Having signs and symptoms of upper or lower airway obstruction\n* Developing agitation and having communication insufficiency\n* Having an allergy to cold vapor application\n* Having a diagnosis of obstructive pulmonary disease (e.g., COPD, asthma) or heart failure\n* Having a known history of any neurological or psychiatric disease\n* Having a postoperative nasogastric catheter inserted\n* Having received preoperative diagnoses associated with nausea, vomiting, or dyspnea","ALL","18 Years",{"count":58,"type":59},66,"ESTIMATED","INTERVENTIONAL",[62],"NA","Cold vapor application is considered a promising intervention with the potential to alleviate side effects associated with anesthesia and surgery in the postoperative period. This study aims to determine the effect of cold vapor inhalation on dyspnea, thirst, nausea, and physiological parameters following laparoscopic inguinal hernia surgery.\n\nHypotheses (H1);\n\nH1a: Patients administered cold vapor will report lower dyspnea severity compared to the control group.\n\nH1b: Patients administered cold vapor will report lower thirst levels compared to the control group.\n\nH1c: Patients administered cold vapor will report lower nausea severity compared to the control group.\n\nH1d: Patients administered cold vapor will show significant differences in physiological parameters compared to the control group.",[65],"Patients Undergoing Laparoscopic Inguinal Hernia Repair",[67,68,69,70,71,72,73,74,75],"PACU","Laparoscopy","inguinal hernia","cold vapor","dyspnea","thirst","nausea","physiological parameters","surgery","NOT_YET_RECRUITING","2026-01-15",{"date":79,"type":80},"2026-01-16","ACTUAL",{"date":82,"type":59},"2025-12-20",{"date":84,"type":59},"2026-09-01",{"name":5,"class":6},1]