[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"recruitment\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:recruitment":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,7,0,[8,41,65,97,124,153,176],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100633326","stepwise-peep-vs-sustained-inflation-in-bariatric-surgery-patients-100633326",false,"NCT07525232","Stepwise PEEP vs Sustained Inflation in Bariatric Surgery Patients","Comparison of Stepwise PEEP vs Sustained Inflation Recruitment Maneuvers on Postoperative Oxygenation and Atelectasis in Bariatric Surgery Patients","Inclusion Criteria:\n\n1. Anesthesiologists (ASA) physical status II, of either sex Age ≥18 y.\n2. Undergoing laparoscopic bariatric surgeries; sleeve gastrectomy, mini gastric bypass\n3. BMI (35-60)\n\nExclusion Criteria:\n\n1. Pre-existing severe pulmonary disease\n2. Baseline hypoxemia SpO₂ \\\u003C92% on room air\n3. History of barotrauma\n4. Previous pneumothorax\n5. Known pulmonary bullae or emphysematous blebs","ALL","18 Years",{"count":19,"type":20},100,"ESTIMATED","INTERVENTIONAL",[23],"NA","Male and female patients Undergoing laparoscopic bariatric surgeries will be subjected for lung recruitment at end of surgery before emergence from anesthesia by two different methods . to evaluate which might be safer and more effective",[26,27],"Recruitment","Bariatric Surgery Candidate","RECRUITING","2026-04-07",{"date":31,"type":32},"2026-04-13","ACTUAL",{"date":34,"type":32},"2026-03-19",{"date":36,"type":20},"2026-11-01",{"name":38,"class":39},"Ain Shams University","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":45,"acronym":46,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":50,"briefSummary":51,"conditions":52,"keywords":53,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":56,"lastUpdatePostDateStruct":57,"startDateStruct":59,"completionDateStruct":61,"leadSponsor":63,"locationsCount":40},"100615263","optimizing-strategies-to-maximize-patient-recruitment-yield-100615263","NCT07290335","Optimizing Strategies to Maximize Patient Recruitment Yield","OSPREY","Inclusion Criteria for primary studies that are recruiting participants:\n\n* All studies using the MyChart recruitment service are eligible, including both clinical trials and observational studies.\n\nExclusion Criterion for primary studies that are recruiting participants:\n\n* Not using MyChart for recruitment.\n* At least 500 messages sent, 125 for each arm\n\nInclusion Criteria for patients:\n\n* All patients receiving messages via MyChart will be included\n* Potential eligibility for a study using MyChart requirement based on the planned query\u002Fcriteria for that study.\n\nExclusion Criteria for patients:\n\n* Minor\n* Excluded from primary study that is recruiting participants.",{"count":49,"type":20},100000,[23],"This platform trial aims to evaluate the effectiveness of different messaging strategies within a MyChart messaging program for research recruitment. MyChart is a patient portal system within the Electronic Medical Record (EMR), and messages can be sent directly to patients about research opportunities.",[26],[54,55],"Research recruitment","Patient portal-based communication","2026-02-23",{"date":58,"type":32},"2026-02-25",{"date":60,"type":32},"2026-02-19",{"date":62,"type":20},"2027-04",{"name":64,"class":39},"Emory University",{"id":66,"slug":67,"hasResults":11,"nctId":68,"briefTitle":69,"officialTitle":70,"acronym":71,"eligibilityCriteria":72,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":73,"enrollmentInfo":74,"targetDuration":4,"studyType":21,"phases":76,"briefSummary":77,"conditions":78,"keywords":83,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":40},"100608916","eit-guided-peep-titration-versus-standard-ventilation-in-bariatric-surgery-100608916","NCT07207772","EIT-guided PEEP Titration Versus Standard Ventilation in Bariatric Surgery","Prevention of Postoperative Pulmonary Complications in Patients Undergoing Laparoscopic Gastric Sleeve Resection by PEEP Titration Based on EIT: A Randomized Controlled Study","EIT","Inclusion Criteria:\n\n1. Age between 18 and 65 years;\n2. Plan to receive laparoscopic bariatric surgery under general anesthesia;\n3. American Society of Anaesthesiologists (ASA) physical status I-III;\n4. BMI between 30 and 55 kg\u002Fm2;\n5. Voluntary participation in this study and signing of an informed consent form.\n\nExclusion Criteria:\n\n1. History of smoking or previous thoracic surgery;\n2. Invasive mechanical ventilation within 30 days;\n3. Pregnancy;\n4. Allergy to EIT electrodes;\n5. Persistent hemodynamic instability or refractory shock;\n6. Severe cardiopulmonary disease (e.g., severe COPD (Chronic obstructive pulmonary disease), NYHA (New York Heart Association) Class III or IV, acute coronary syndrome, or sustained ventricular tachycardia);\n7. Severe pulmonary hypertension (systolic pulmonary artery pressure \\>40 mmHg);\n8. Increased intracranial pressure, intracranial injury\u002Ftumor, or neuromuscular disorders;\n9. Conversion to laparotomy;\n10. Planned transfer to intensive care unit after surgery.","65 Years",{"count":75,"type":20},118,[23],"This study is a prospective, single-center, single-blind, randomized controlled clinical trial. Patients scheduled for laparoscopic bariatric surgery will be selected and randomly assigned to either the EIT-guided individualized PEEP group (Group P-eit) or the control group (Group P-8). Group P will be ventilated using the PEEP value determined by EIT, while Group C will be ventilated with a fixed PEEP value of 8 cmH2O.The primary outcome is the incidence of postoperative pulmonary complications (PPCs) within 72 hours after surgery.",[79,80,26,81,82],"Electrical Impedance Tomography (EIT)","Postoperative Pulmonary Complications (PPCs)","Mechanical Ventilation Complication","Obesity",[79,80,84,85,86,87],"Lung protective ventilation strategy","Recruitment manoeuvre(RM)","Conventional lung-protective ventilation","bariatric","2025-09-27",{"date":90,"type":32},"2025-10-06",{"date":92,"type":32},"2025-07-28",{"date":94,"type":20},"2027-12-31",{"name":96,"class":39},"Jianbo Wu",{"id":98,"slug":99,"hasResults":11,"nctId":100,"briefTitle":101,"officialTitle":101,"acronym":4,"eligibilityCriteria":102,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":73,"enrollmentInfo":103,"targetDuration":4,"studyType":21,"phases":105,"briefSummary":106,"conditions":107,"keywords":110,"overallStatus":114,"whyStopped":4,"lastUpdateSubmitDate":115,"lastUpdatePostDateStruct":116,"startDateStruct":118,"completionDateStruct":120,"leadSponsor":122,"locationsCount":40},"100597631","evaluation-of-recruitment-effectiveness-in-patients-with-obstructive-sleep-apnea-syndrome-using-lung-ultrasound-100597631","NCT07061002","Evaluation of Recruitment Effectiveness in Patients With Obstructive Sleep Apnea Syndrome Using Lung Ultrasound","Inclusion Criteria:\n\n* Patients aged 18-65\n* American Society of Anesthesia I-III\n* Patients with consent to participate\n* Patients with preoperative OSA diagnosis (polysomnography or STOP-BANG≥3)\n\nExclusion Criteria:\n\n* American Society of Anesthesia \\>IV\n* Patients planned for postoperative intensive care follow-up 3. Cardiac surgery\n* Anesthesia outside the operating room\n* History of neuromuscular disease\n* Emergency surgical application\n* Invasive airway surgeries (pharynx, larynx)\n* Lung surgeries (pneumonectomy, lobectomy, etc.) 9. Presence of pregnancy",{"count":104,"type":20},66,[23],"Patients with obstructive sleep apnea syndrome are at higher risk for respiratory complications after surgery. Oxygen depletion and respiratory distress are common in patients with obstructive sleep apnea syndrome. In this study, the effectiveness of the recruitment maneuver applied in the postoperative period will be investigated via lung ultrasound. Recruitment is a technique performed to improve the oxygen levels of patients. Patients diagnosed with obstructive sleep apnea syndrome between the ages of 18-65 will be included in the study and anesthesia and surgical procedures will be followed. The aim of the study is to compare the pulmonary complication rates between patients who underwent recruitment and those who did not, and to examine the effects of factors such as age and gender on these complications via lung ultrasound.",[108,109,26],"Postoperative Atelectasis","Lung Ultrasonography Score",[111,112,113],"Postoperative Pulmonary Atelectases","lung ultrasound score","recruitment maneuver","NOT_YET_RECRUITING","2025-07-02",{"date":117,"type":32},"2025-07-11",{"date":119,"type":20},"2025-07-25",{"date":121,"type":20},"2026-07-01",{"name":123,"class":39},"Istanbul University - Cerrahpasa",{"id":125,"slug":126,"hasResults":11,"nctId":127,"briefTitle":128,"officialTitle":129,"acronym":130,"eligibilityCriteria":131,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":132,"targetDuration":4,"studyType":21,"phases":134,"briefSummary":135,"conditions":136,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":147,"completionDateStruct":149,"leadSponsor":151,"locationsCount":40},"100561279","clinical-trial-recruitment-and-retention-strategies-for-family-members-in-the-icu-100561279","NCT06588101","Clinical Trial Recruitment and Retention Strategies for Family Members in the ICU","Clinical Trial Recruitment and Retention Strategies for Family Members in the Intensive Care Unit: A Study Within A Trial Randomized Design","SWAT","Inclusion Criteria:\n\n* Has family member admitted to an intensive care unit.\n* Expected hospital stay \\> 48 hours\n* Able to participate in English or French\n\nExclusion Criteria:\n\n* Has another family member participating in the trial\n* Repeat admissions within the study period",{"count":133,"type":20},160,[23],"There is a need to identify strategies that improve the conduct of clinical trials involving family members of intensive care unit (ICU) patients. The purpose of the present study is to evaluate recruitment and retention strategies for clinical trials involving family members of ICU patients. 4 strategies (2 recruitment and 2 retention) will be tested. Investigators will integrate the strategies into three existing studies that involve family members of ICU patients. Participants will be randomized using a 2x2 factorial design. The co-primary outcomes are recruitment percentage (participants enrolled\u002Fparticipants approached) and retention percentage (participants completing follow-up\u002Fparticipants enrolled).",[137,26,138,139,140,141,142,143],"Family Members","Clinical Study","Retention","Recruitment of Participants","Study Enrollment","Retention of Participants","Compensation Incentives","2025-05-29",{"date":146,"type":32},"2025-06-04",{"date":148,"type":32},"2024-05-01",{"date":150,"type":20},"2026-12-31",{"name":152,"class":39},"Lady Davis Institute",{"id":154,"slug":155,"hasResults":11,"nctId":156,"briefTitle":157,"officialTitle":158,"acronym":159,"eligibilityCriteria":160,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":161,"targetDuration":4,"studyType":163,"phases":4,"briefSummary":164,"conditions":165,"keywords":4,"overallStatus":114,"whyStopped":4,"lastUpdateSubmitDate":167,"lastUpdatePostDateStruct":168,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":40},"100569036","positive-expiratory-pressure-pep-and-continuous-high-frequency-oscillation-chfo-on-lung-recruitment-using-electrical-impedance-tomography-eit---the-pep-recruit-study-100569036","NCT06689020","Positive Expiratory Pressure (PEP) and Continuous High-frequency Oscillation (CHFO) on Lung RECRUITment Using Electrical Impedance Tomography (EIT) - The PEP-RECRUIT Study","Effect of Continuous High-frequency Oscillation (CHFO) and Continuous Positive Expiratory Pressure (CPEP) Therapy on Lung RECRUITment Using Electrical Impedance Tomography (EIT) - The PEP-RECRUIT Study","PEP-RECRUIT","Inclusion Criteria:\n\n* Patients who require pulmonary expansion and airway clearing as per clinical indication\n* Patients who provide valid informed consent according to local regulations\n* PaO2\u002FFiO2 \\\u003C 200 mmHg at inclusion\n* Patient on the Airway Care Score (ACS) \\\u003C 7\n\nExclusion Criteria:\n\n* Refuse to participate\n* Age \\\u003C 18 years\n* Hemodynamic instability, defined as systolic arterial pressure \\\u003C 90 mmHg or mean pressure \\\u003C 60 mmHg\n* Contraindication to using an EIT (i.e., pacemaker or defibrillator)\n* Inability to properly position the EIT device for anatomical reasons",{"count":162,"type":20},26,"OBSERVATIONAL","This single-center observational study aims to assess the effects of continuous high-frequency oscillation (CHFO) and continuous positive expiratory pressure (CPEP) therapy on lung recruitment using electrical impedance tomography (EIT) in spontaneously breathing patients admitted to the intensive care unit.",[26,166],"Respiratory Failure","2024-11-12",{"date":169,"type":32},"2024-11-14",{"date":171,"type":20},"2024-12-01",{"date":173,"type":20},"2025-07-01",{"name":175,"class":39},"University of Genova",{"id":177,"slug":178,"hasResults":11,"nctId":179,"briefTitle":180,"officialTitle":180,"acronym":4,"eligibilityCriteria":181,"healthyVolunteers":182,"sex":183,"minAge":17,"maxAge":184,"enrollmentInfo":185,"targetDuration":4,"studyType":163,"phases":4,"briefSummary":187,"conditions":188,"keywords":189,"overallStatus":114,"whyStopped":4,"lastUpdateSubmitDate":195,"lastUpdatePostDateStruct":196,"startDateStruct":198,"completionDateStruct":200,"leadSponsor":202,"locationsCount":40},"100555403","multicenter-quantitative-and-qualitative-study-of-the-determinants-of-participation-in-a-cytomegalovirus-preventive-vaccine-study-in-france-in-women-aged-18-to-40-years-old-100555403","NCT06511635","Multicenter Quantitative and Qualitative Study of the Determinants of Participation in a Cytomegalovirus Preventive Vaccine Study in France in Women Aged 18 to 40 Years Old.","Inclusion Criteria:\n\n* Womens between 18 to 40 included in CMVCTORY vaccine trial\n\nExclusion Criteria:\n\n* Refusal",true,"FEMALE","40 Years",{"count":186,"type":20},306,"During a vaccine clinical trial of Cytomegalovirus (CMV) vaccine, one of the participants' motivations was to prevent an infection responsible for malformations in a future child. Would their attitude towards a vaccine trial be the same in the context of a vaccine designed to protect them individually? By improving the knowledge of clinical research and determinants in women aged 18 to 40, this study could improve recruitment methods in this specific population for future vaccine trials within the CIC1408 infectious diseases and vaccinology area at Saint-Etienne University Hospital.",[26],[190,191,192,193,194],"Recruitment methods","Determinants","CMVCTORY vaccine trial","women's participation","vaccine trial","2024-07-15",{"date":197,"type":32},"2024-07-22",{"date":199,"type":20},"2024-09",{"date":201,"type":20},"2024-11",{"name":203,"class":39},"Centre Hospitalier Universitaire de Saint Etienne"]