[{"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":76},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,40],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":4,"enrollmentInfo":17,"targetDuration":4,"studyType":20,"phases":21,"briefSummary":23,"conditions":24,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":4},"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":18,"type":19},20,"ESTIMATED","INTERVENTIONAL",[22],"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.",[25,26,27],"Laparoscopic Surgical Procedures","Airway Control","Anesthesia","NOT_YET_RECRUITING","2026-02-02",{"date":31,"type":32},"2026-02-06","ACTUAL",{"date":34,"type":19},"2026-02-01",{"date":36,"type":19},"2027-03-01",{"name":38,"class":39},"Medical University of Lodz","OTHER",{"id":41,"slug":4,"hasResults":10,"nctId":42,"briefTitle":43,"officialTitle":44,"acronym":45,"eligibilityCriteria":46,"healthyVolunteers":10,"sex":15,"minAge":16,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":20,"phases":50,"briefSummary":51,"conditions":52,"keywords":57,"overallStatus":65,"whyStopped":4,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":69,"completionDateStruct":71,"leadSponsor":73,"locationsCount":75},"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":49,"type":19},660,[22],"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.",[53,54,55,56,26],"Mechanical Ventilator Weaning","Acute Brain Injury","Altered Level of Consciousness","Mechanical Ventilation",[58,59,60,61,62,63,64],"Coma","Intensive care units","Critical care","Stroke","Traumatic brain injury","Anoxic ischemic encephalopathy","Glasgow coma scale","RECRUITING","2025-09-23",{"date":68,"type":32},"2025-09-24",{"date":70,"type":32},"2020-02-09",{"date":72,"type":19},"2027-10-13",{"name":74,"class":39},"University Hospital, Clermont-Ferrand",21,""]