[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"airway-control\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:airway-control":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"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":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":4},"100623079","evaluation-of-saco-vlma-for-general-anesthesia-for-laparoscopic-procedures-100623079",false,"NCT07391969","Evaluation of SaCo VLMA for General Anesthesia for Laparoscopic Procedures","Evaluation of New Supraglottic Airway Device - SaCo VLMA for General Anesthesia for Laparoscopic Procedures","Inclusion Criteria:\n\n* Patients undergoing elective surgery under general anesthesia for laparoscopic surgery of predicting lasting no longer than about 1 hour.\n* Age \\>18 years.\n* ASA I-III.\n* Present ordinary airway\n\nExclusion Criteria:\n\n* Not meeting the above criteria\n* Presenting 3 predictors of a difficult airway (Mallampatti class III or IV; thyromental distance \\\u003C6 cm, sternomental distance \\\u003C12.5 cm, distance between incisors \\\u003C4.0 cm, bite test II or III, cervical mobility \\\u003C90o).\n* Gestation\n* Allergy to any drug included in the protocol.\n* Present risk factors for bronchial aspiration\n\n  \\- Presenting with preoperative sore throat\n* Present severe respiratory, coronary or cerebral vascular pathology.","ALL","18 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"NA","Evaluation of new supraglottic device SaCo VLMA for laparoscopic procedures under general anesthesia in comparison with other airway management methods including other supraglottic devices. The parameters noted will be: demographic data, time for placement of SGA counted from moment of grabbing device by operator to correct placement, subjective evaluation of ease of insertion of SGA in 5 step Borg scale, peak pressure, lung compliance, achieved tidal volume before creating pneumoperitoneum, after creating pneumoperitoneum, visualization of glottis on monitor of camera or fiberoptic scope.",[26,27,28],"Laparoscopic Surgical Procedures","Airway Control","Anesthesia","NOT_YET_RECRUITING","2026-02-02",{"date":32,"type":33},"2026-02-06","ACTUAL",{"date":35,"type":20},"2026-02-01",{"date":37,"type":20},"2027-03-01",{"name":39,"class":40},"Medical University of Lodz","OTHER",{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":53,"conditions":54,"keywords":59,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"100368678","brain-injured-patients-extubation-readiness-study-100368678","NCT04080440","Brain-injured Patients Extubation Readiness Study","Stepped Wedge Cluster Randomised Controlled Trial to Assess the Readiness of Extubation in Brain-injured Patients Using a Clinical Score","Biper","Inclusion Criteria:\n\n* Acute cerebral lesion with a Glasgow Coma Scale \\\u003C13 needing admission in ICU and mechanical ventilation with tracheal intubation for neurological cause : cerebrovascular stroke either ischemic or hemorrhagic including aneurysmal subarachnoid hemorrhage, traumatic brain injury, anoxo ischemic encephalopathy after cardiac arrest or brain tumour\n* Mechanical ventilation more than 48 hours\n* 18 to 75 years old\n* Neurological stability with no intracranial hypertension with minimal sedation\n* Glasgow Coma Scale motor response \\\u003C 6\n* Spontaneous breathing trial succeeded\n* First extubation attempt\n\nExclusion Criteria:\n\n* Posterior cranial fossa lesion\n* Admission for status epilepticus or central nervous system infection\n* Spinal cord injury (tetraplegia or paraplegia)\n* Uncontrolled status epilepticus or uncontrolled central nervous system infection\n* Care limitation plan\n* Chronic respiratory failure defined as ambulatory oxygen therapy or pressure support ventilation and\u002For proven COPD and\u002For ambulatory non-invasive CPAP therapy for sleep apnoea syndrome\n* More than 3 failed spontaneous breathing trials\n* Significant chest trauma (more than 2 broken ribs \u002F broken sternum \u002F with an indication of open thoracic surgery)\n* Surgery planned within 7 days\n* Tracheotomy or previous extubation outside of the protocol\n* Previous compromised upper airway permeability\n* Pregnant or breastfeeding woman\n* Adult under the protection of the law or without social assurance system\n* Inclusion in another clinical study about mechanical ventilation or weaning","75 Years",{"count":51,"type":20},660,[23],"The BIPER study is a stepped wedge cluster randomised clinical trial aiming to decrease extubation failure in critically-ill brain-injured patients with residual impaired consciousness using a simple clinical score.",[55,56,57,58,27],"Mechanical Ventilator Weaning","Acute Brain Injury","Altered Level of Consciousness","Mechanical Ventilation",[60,61,62,63,64,65,66],"Coma","Intensive care units","Critical care","Stroke","Traumatic brain injury","Anoxic ischemic encephalopathy","Glasgow coma scale","RECRUITING","2025-09-23",{"date":70,"type":33},"2025-09-24",{"date":72,"type":33},"2020-02-09",{"date":74,"type":20},"2027-10-13",{"name":76,"class":40},"University Hospital, Clermont-Ferrand",21]