[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"geriatric-population\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:geriatric-population":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,50,82,106,129],{"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":28,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":38,"lastUpdatePostDateStruct":39,"startDateStruct":42,"completionDateStruct":44,"leadSponsor":46,"locationsCount":49},"100644633","thirst-for-knowledge-100644633",false,"NCT07670767","Thirst for Knowledge","Thirst for Knowledge: A Hydration Education Program for Geriatrics","Inclusion Criteria:\n\nBe a current resident at Cornwall Manor in the independent living unit Understand English Be literate to 5th grade level and up Ages 60+ years old Self report that they do not have a diagnosis of heart failure, dialysis, end stage renal failure and\u002For Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH) Have the ability to drink thin liquids Be their own legal guardian\n\nExclusion Criteria:\n\nIndividuals with a diagnosis of heart failure, dialysis, end-stage renal failure and\u002For Syndrome of Inappropriate Antidiuretic Hormone secretion (SIADH) will be excluded. This is due to increasing water intake with participants with these conditions could be potentially harmful or life threatening.",true,"ALL","60 Years",{"count":20,"type":21},30,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of this project is to determine the impact of hydration education on participant knowledge and water intake for residents in the independent living unit at Cornwall Manor. Therefore, we aim to look at the impact of education as a tool to improve overall hydration among the geriatric population.",[27],"Geriatric Population",[29,30,31,32,33,34,35,36],"hydration","community-based","education","Geriatrics","older adults","dehydration","low water intake","water accessibility","RECRUITING","2026-06-22",{"date":40,"type":41},"2026-06-26","ACTUAL",{"date":43,"type":41},"2026-05-11",{"date":45,"type":21},"2026-08-14",{"name":47,"class":48},"Duquesne University","OTHER",1,{"id":51,"slug":52,"hasResults":11,"nctId":53,"briefTitle":54,"officialTitle":55,"acronym":4,"eligibilityCriteria":56,"healthyVolunteers":11,"sex":17,"minAge":57,"maxAge":4,"enrollmentInfo":58,"targetDuration":60,"studyType":61,"phases":4,"briefSummary":62,"conditions":63,"keywords":67,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":73,"lastUpdatePostDateStruct":74,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":49},"100622100","the-cognitive-functional-relationship-in-geriatric-hand-forearm-injuries-100622100","NCT07379229","The Cognitive-Functional Relationship in Geriatric Hand-Forearm Injuries","Investigation of the Relationship Between Cognitive and Functional Status in Geriatric Patients With Hand-Forearm Injuries","Inclusion Criteria:\n\n* Being over 65 years of age\n* Having sufficient communication skills and auditory-visual abilities to complete cognitive tests\n\nExclusion Criteria:\n\n* Inability to perform functional tests due to active wounds, open fractures, or severe pain\n* Inability to administer cognitive tests due to aphasia or severe hearing or visual impairment","66 Years",{"count":59,"type":21},34,"12 Weeks","OBSERVATIONAL","Considering the complex structure of hand-forearm injuries and the long rehabilitation process, it is important to investigate factors associated with recovery in geriatric individuals. Therefore, this study aimed to examine the relationship between cognitive status and functional outcomes in geriatric individuals with hand-forearm injuries.",[27,64,65,66],"Cognitive Ability","Functional Abilities","Hand Injuries",[68,69,70,71],"geriatric population","hand Injuries","functional outcome","cognitive function","NOT_YET_RECRUITING","2026-01-30",{"date":75,"type":41},"2026-02-03",{"date":77,"type":21},"2026-02-23",{"date":79,"type":21},"2026-12-30",{"name":81,"class":48},"Pamukkale University",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":22,"phases":92,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":49},"100620924","height-based-and-conventional-spinal-anaesthetic-dosing-in-geriatric-patients-100620924","NCT07363941","HEIGHT-BASED AND CONVENTIONAL SPINAL ANAESTHETIC DOSING IN GERIATRIC PATIENTS","COMPARISON OF HEMODYNAMIC AND ANAESTHETIC OUTCOMES BETWEEN HEIGHT-BASED AND CONVENTIONAL SPINAL ANAESTHETIC DOSING IN GERIATRIC PATIENTS UNDERGOING LOWER LIMB ORTHOPAEDIC SURGERIES","Inclusion Criteria:\n\nIndividuals aged 60 to 80 years. Either gender (male or female). Patients who are ASA physical status I-III. Individuals scheduled to undergo elective lower limb orthopaedic surgeries (e.g., fracture fixation, total knee replacement, open reduction and internal fixation).\n\nPatients planned to receive spinal anaesthesia as the primary anaesthetic technique.\n\nThose who provide informed written consent for participation in the study.\n\nExclusion Criteria:\n\nIndividuals exhibiting a stature inferior to 150 cm. Patients receiving anti-hypertensive drugs or those on beta blockers or beta-agonists.\n\nPatients with a history of neurological disease like CVA or Parkinsonism. Patients presenting with sepsis (≥ 2 positive SIRS criteria with positive aseptically obtained blood or wound culture).\n\nPatients with a history of coagulation disorders like haemophilia or vWD or those with a history of anti-platelet drug intake in the last 2 weeks.\n\nIndividuals possessing a documented history of hypersensitivity reactions to pharmacological agents utilized in the research.\n\nPatients who will be diagnosed with a skin infection at the spinal needle puncture site.\n\nPatients undergoing emergency orthopaedic procedures requiring immediate intervention","80 Years",{"count":91,"type":21},104,[24],"The goal of this clinical trial is to find out whether height-based dosing of spinal anaesthesia provides better hemodynamic stability and anesthetic outcome than conventional fixed dosing in elderly patients undergoing lower limb orthopaedic surgery.The main questions this study aims to answer are:\n\n1. Does height-based spinal anaesthetic dosing reduce the risk of hypotension and bradycardia during surgery as compared to conventional fixed dosing?\n2. Does it improve anaesthetic outcomes, such as the onset and duration of sensory and motor block?",[27,95,96],"Spinal Anesthesia Induced Hypotension","Spinal Anesthesia in Elderly Patients","2026-01-15",{"date":99,"type":41},"2026-01-23",{"date":101,"type":41},"2026-01-03",{"date":103,"type":21},"2026-05-04",{"name":105,"class":48},"Shaheed Mohtarma Benazir Bhutto Institue of Trauma",{"id":107,"slug":108,"hasResults":11,"nctId":109,"briefTitle":110,"officialTitle":111,"acronym":4,"eligibilityCriteria":112,"healthyVolunteers":11,"sex":17,"minAge":113,"maxAge":4,"enrollmentInfo":114,"targetDuration":116,"studyType":61,"phases":4,"briefSummary":117,"conditions":118,"keywords":4,"overallStatus":72,"whyStopped":4,"lastUpdateSubmitDate":120,"lastUpdatePostDateStruct":121,"startDateStruct":123,"completionDateStruct":125,"leadSponsor":127,"locationsCount":4},"100581132","opioid-free-anesthesia-and-quality-of-recovery-after-general-anesthesia-100581132","NCT06846333","Opioid-free Anesthesia and Quality of Recovery After General Anesthesia","Effect of Opioid-free Anesthesia Protocol on Quality of Recovery After Major Surgery in Geriatric Patients","Inclusion Criteria:\n\n* Patients aged 65 and older\n* Undergoing major elective non-cardiac surgery under general anesthesia\n* Classified as ASA I-II-III\n* With sufficient cognitive ability to complete a questionnaire were included in the study\n\nExclusion Criteria:\n\n* Patients requiring rapid sequence induction for emergency cases\n* Those with severe psychiatric or cognitive disorders preventing questionnaire evaluation\n* A body mass index \\\u003C 18 or \\> 39 kg\u002Fm²\n* Allergy or contraindication to any drug included in the study\n* A history of chronic pain or chronic opioid use\n* Uncontrolled epilepsy, decompensated heart failure\n* Chronic kidney or liver failure\n* Preoperative bradycardia with atrioventricular block (2nd or 3rd degree)\n* Heart rate \\\u003C 50 bpm due to chronic beta-blocker therapy\n* Those using medications that prolong the QT interval\n* Patients whose anesthesia regimen was intraoperatively changed (from opioid-free to opioid-containing anesthesia)","65 Years",{"count":115,"type":21},60,"3 Days","This study aimed to evaluate the effect of an opioid-free anesthesia protocol on postoperative recovery quality in patients aged 65 years and older undergoing major surgery. Recovery quality was assessed using the Quality of Recovery-15 (QoR-15) questionnaire. Findings are expected to contribute to optimizing anesthesia practices in the elderly population by improving recovery quality and reducing opioid-related side effects.",[119,27],"Opioid-free Anesthesia","2025-02-25",{"date":122,"type":41},"2025-02-26",{"date":124,"type":21},"2025-02-20",{"date":126,"type":21},"2025-04-30",{"name":128,"class":48},"Selcuk University",{"id":130,"slug":131,"hasResults":11,"nctId":132,"briefTitle":133,"officialTitle":134,"acronym":4,"eligibilityCriteria":135,"healthyVolunteers":16,"sex":17,"minAge":113,"maxAge":136,"enrollmentInfo":137,"targetDuration":4,"studyType":22,"phases":139,"briefSummary":141,"conditions":142,"keywords":4,"overallStatus":37,"whyStopped":4,"lastUpdateSubmitDate":145,"lastUpdatePostDateStruct":146,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":49},"100579064","phase-4-effect-of-dexamethasone-on-post-spinal-hypotension-100579064","NCT06819436","Effect of Dexamethasone on Post-spinal Hypotension","Effect of Dexamethasone on Post-spinal Hypotension in Geriatric Patients Undergoing Orthopaedic Surgery at Tertiary Care Hospital Karachi.","Inclusion Criteria:\n\nPatient undergoing orthopedic surgery in spinal anesthesia. ASA ≤ 2.\n\nExclusion Criteria:\n\nPatients with history of cardiac arrhythmias. Patients with history of acute coronary syndrome. Patient with history of polytrauma. Patients with contraindication to SA (e.g., coagulopathy, thrombocytopenia, allergy to local anesthetic agent) and those on steroids or serotonin related medications (e.g., selective serotonin reuptake inhibitor) will be excluded.","85 Years",{"count":138,"type":21},170,[140],"PHASE4","The goal of this clinical trial is to learn if intravenous dexamethasone is effective for prevention of post spinal hypotension in geriatric population undergoing orthopedic surgeries. The main question aim to answer is:\n\nDoes intravenous dexamethasone in participants undergoing orthopedic procedures of lower limb under spinal anesthesia prevents post spinal hypotension? Researchers are comparing two groups of participants\n\n* Participants in (Dexamethasone Group) Group D are receiving intravenous dexamethasone 8mg preoperatively\n* Participants in (Placebo Group) Group P are receiving placebo preoperatively.",[143,27,144],"Post Spinal Anaesthesia Hypotension","Orthopedic Surgeries","2025-02-05",{"date":147,"type":41},"2025-02-11",{"date":149,"type":21},"2025-02",{"date":151,"type":21},"2025-05",{"name":105,"class":48}]