[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Memorial Hermann Health System\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":78},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,49],{"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":30,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":37,"lastUpdatePostDateStruct":38,"startDateStruct":41,"completionDateStruct":43,"leadSponsor":45,"locationsCount":48},"100649585","lavender-sandalwood-aromatherapy-study-100649585",false,"NCT07737392","Lavender Sandalwood Aromatherapy Study","Does Aromatherapy Improve Mood and Reduce Pain in Women After Scheduled Cesarean Procedures?","Inclusion Criteria:\n\n* Patients scheduled for a planned cesarean section\n* Undergoing pre-admission testing\n\nExclusion Criteria:\n\n* Individuals under 18 years of age\n* High-risk pregnancies\n* Patients not admitted to the postpartum unit following delivery\n* Individuals with known allergies to essential oils\n* Patients whose newborns require admission to the NICU\n* Patients originally scheduled for a cesarean section but admitted to the labor and delivery unit before the planned procedure","FEMALE","18 Years",{"count":19,"type":20},182,"ESTIMATED","INTERVENTIONAL",[23],"NA","The purpose of this randomized controlled study is to explore whether lavender sandalwood aromatherapy can support comfort, mood, pain relief, and overall satisfaction for participants recovering from a scheduled cesarean section without complications. The main questions this study aims to answer are:\n\n* How does lavender sandalwood aromatherapy affect participants' mood during postpartum recovery after a cesarean section?\n* Does lavender sandalwood aromatherapy help reduce pain during recovery?\n* Does lavender sandalwood aromatherapy improve participants' overall satisfaction with their recovery experience? Researchers will compare participants who receive lavender-sandalwood aromatherapy with those who do not to determine whether it improves mood, reduces pain, and enhances patient satisfaction.\n\nParticipants will be asked to:\n\n* Wear aromatherapy tabs on their gown for 24 hours.\n* Have the aromatherapy tabs applied 24 hours after the cesarean section and removed 48 hours after the cesarean section.\n* Complete surveys at 24 hours and 48 hours after the cesarean section. This will apply to both the control and intervention groups.",[26,27,28,29],"Pain","Mood","Patient Satisfaction","Scheduled Cesarean Sections",[31,26,27,32,33,34,35],"Post C\u002Fsection","Aromatherapy","Lavender","Sandalwood","Patient satisfaction","NOT_YET_RECRUITING","2026-08-10",{"date":39,"type":40},"2026-08-12","ACTUAL",{"date":42,"type":20},"2026-09",{"date":44,"type":20},"2027-12",{"name":46,"class":47},"Memorial Hermann Health System","OTHER",1,{"id":50,"slug":51,"hasResults":11,"nctId":52,"briefTitle":53,"officialTitle":53,"acronym":54,"eligibilityCriteria":55,"healthyVolunteers":11,"sex":56,"minAge":17,"maxAge":57,"enrollmentInfo":58,"targetDuration":4,"studyType":21,"phases":60,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":36,"whyStopped":4,"lastUpdateSubmitDate":70,"lastUpdatePostDateStruct":71,"startDateStruct":73,"completionDateStruct":75,"leadSponsor":77,"locationsCount":48},"100577650","phase-1-safety-of-a-second-dose-of-tenecteplase-in-selected-acute-ischemic-stroke-patients-not-responding-to-the-first-dose-100577650","NCT06801054","Safety Of A Second Dose Of Tenecteplase In Selected Acute Ischemic Stroke Patients Not Responding To The First Dose","DoubleDoseTNK","Inclusion Criteria:\n\n* Signs and symptoms suggestive of acute ischemic stroke\n* Age \\> 18 and \\\u003C 80 years\n* Time from LKN \\\u003C 3 hrs (first dose) and \\\u003C4.5 hours (second dose)\n* NIHSS \\> 6 and (for both first and second dose)\n* CT at baseline and prior to second dose shows no evidence of intracranial hemorrhage and has an ASPECTS score \\> 6\n* Patient\u002Flegally authorized representative has signed the Informed Consent Form\n\nExclusion Criteria:\n\n* Patients with LVO or MeVO for whom EVT is intended at any time before the second dose of TENECTEPLASE\n* At the time of the second dose, NIHSS is \\\u003C 6\n* Systolic blood pressure \\> 180 at the time of either dose of TENECTEPLASE\n* Pre-stroke mRS \\> 2\n* Patients receiving more than one antiplatelet agent during the 48 hours prior to enrollment\n* Active internal bleeding\n* Patients with undiagnosed significant cognitive impairment or known cerebral amyloid angiopathy\n* Patients taking lecanemab, donanemab, or other amyloid reduction therapy\n* Known bleeding diathesis\n* Recent use of heparin with PTT \\> control\n* Known hereditary or acquired hemorrhagic diathesis, coagulation factor deficiency; known administration of warfarin within 24 hours or suspected use and INR \\> 1.5.\n* Use of one of the direct oral anticoagulants within the last 48 hours (dabigatran, rivaroxaban, apixaban, edoxaban)\n* Treatment with a thrombolytic within the last 3 months prior to enrollment\n* Baseline platelet count \\\u003C 100,000\u002FμL (results must be available prior to treatment)\n* Baseline blood glucose \\> 400 mg\u002FdL (22.20 mmol\u002FL)\n* Baseline blood glucose \\\u003C 50 mg\u002FdL needs to be normalized prior to enrollment\n* Intracranial or intraspinal surgery or trauma within 2 months\n* History of acute ischemic stroke in the last 90 days\n* History of hemorrhagic stroke\n* Presumed septic embolus; suspicion of bacterial endocarditis\n* Other serious, advanced, or terminal illness (investigator's judgment) or life expectancy is less than 6 months\n* Pregnant\n* Current participation in another investigational drug or device study\n* Known hypersensitivity or allergy to any ingredients of TENECTEPLASE","ALL","80 Years",{"count":59,"type":20},20,[61],"PHASE1","In this pilot safety study, the investigators will give a second dose of Intravenous Tenecteplase (IV TNK) to patients receiving the initial TNK dose within 3 hrs of last known normal (LKN), have a baseline National Institutes of Health Stroke Scale (NIHSS) \\> 6, and who do not clinically improve within 45 minutes of the first dose, or who improve but then deteriorate, and can still be treated within 4.5 hours from LKN. Patients will require a second computed tomography (CT) scan to rule out any bleeding, and meet the usual inclusion and exclusion criteria for TNK treatment, before the second dose which must be given within 4.5 hrs of LKN. Both TNK doses will be 0.25 mg\u002Fkg. The initial TNK dose may be given on the Mobile Stroke Unit (MSU) or Emergency Department (ED), and the second dose in the ED. Informed consent will be obtained before the second dose is given.\n\nThe primary outcome will be symptomatic intracranial hemorrhage (sICH) (SITS-MOST criteria) or serious systemic bleeding within 36 hours. Secondary outcomes will be any intracranial hemorrhage, any bleeding, discharge NIHSS and modified Rankin Score (mRS), and mRS at 90 days (sliding dichotomy).\n\n20 patients will be enrolled. Enrollment will be stopped if more than 3 sICH occur (\\> 80% confidence that sICH rate is \\> 5%. If successful, this study will be followed by a larger phase 2b controlled safety confirmation and pilot efficacy study,",[64],"Acute Ischemic Stroke",[66,67,68,69],"stroke","tenecteplase","mobile stroke unit","acute ischemic stroke","2025-06-03",{"date":72,"type":40},"2025-06-05",{"date":74,"type":20},"2025-07-01",{"date":76,"type":20},"2026-09-30",{"name":46,"class":47},""]