[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"blood-pressure-measurement-in-pregnancy\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:blood-pressure-measurement-in-pregnancy":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,51,82],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":31,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100624137","arm-position-and-blood-pressure-measurement-accuracy-during-pregnancy-100624137",false,"NCT07405723","Arm Position and Blood Pressure Measurement Accuracy During Pregnancy","Arm Position and Blood Pressure Measurement Accuracy in Pregnancy: A Randomized Controlled Trial","Inclusion Criteria:\n\n* Pregnant women aged 18 to 55 years\n* Singleton or multiple viable intrauterine pregnancy\n* Gestational age corresponding to first, second, or third trimester at the time of enrollment\n* Ability to sit upright comfortably for the duration of blood pressure measurements\n* Ability to understand the study procedures and provide written informed consent\n\nExclusion Criteria:\n\n* Preexisting significant cardiac disease (e.g., arrhythmias, congenital heart disease, severe valvular disease)\n* Chronic kidney disease defined as serum creatinine ≥1.5 mg\u002FdL at enrollment\n* Significant upper limb or shoulder conditions that may affect arm positioning or blood pressure measurement (e.g., lymphedema, fractures, prior surgery, arteriovenous fistula)\n* Neurological or musculoskeletal conditions preventing proper positioning\n* Severe preeclampsia, eclampsia, or other acute medical conditions requiring immediate intervention\n* Major fetal anomaly\n* Intrauterine fetal demise",true,"FEMALE","18 Years","55 Years",{"count":21,"type":22},300,"ESTIMATED","INTERVENTIONAL",[25],"NA","Accurate blood pressure measurement is essential during pregnancy, as blood pressure readings guide clinical decisions related to the diagnosis and management of hypertensive disorders of pregnancy. Clinical guidelines recommend measuring blood pressure with the arm supported at heart level; however, in routine practice, blood pressure is often measured with the arm in non-standard positions.\n\nThis study aims to evaluate how different arm positions affect blood pressure measurements in pregnant women. Pregnant women attending a high-risk pregnancy clinic will undergo blood pressure measurements with the arm placed in several commonly used positions, including supported at heart level, supported on the lap, and unsupported at the side. Each participant will have multiple measurements taken during a single clinic visit.\n\nThe study is designed as a randomized crossover trial with stratification by trimester and chronic hypertension status, allowing each participant to serve as her own control. Participants will be enrolled across all three trimesters of pregnancy, and results will be analyzed separately for each trimester. The primary outcome is the difference in systolic and diastolic blood pressure measurements between arm positions.\n\nThe findings of this study may help improve the accuracy of blood pressure measurement during pregnancy and inform clinical practice regarding optimal measurement techniques.",[28,29,30],"Pregnancy","Blood Pressure Measurement in Pregnancy","Hypertensive Disorder of Pregnancy",[32,28,33,34,35,36,37],"Blood Pressure Measurement","Arm Position","Hypertensive Disorders of Pregnancy","Prenatal Care","Blood Pressure Accuracy","Randomized Crossover Trial","RECRUITING","2026-04-13",{"date":41,"type":42},"2026-04-16","ACTUAL",{"date":44,"type":42},"2026-04-12",{"date":46,"type":22},"2026-12-31",{"name":48,"class":49},"Sheba Medical Center","OTHER_GOV",1,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":60,"studyType":61,"phases":4,"briefSummary":62,"conditions":63,"keywords":66,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":75,"completionDateStruct":77,"leadSponsor":79,"locationsCount":50},"100625448","comparison-of-non-invasive-mean-arterial-blood-pressure-measurements-at-the-arm-and-ankle-during-elective-cesarean-delivery-100625448","NCT07422766","Comparison of Non-Invasive Mean Arterial Blood Pressure Measurements at the Arm and Ankle During Elective Cesarean Delivery.","Observational Study Comparing Non-Invasive Mean Arterial Blood Pressure Measurements at the Arm and Ankle During Elective Cesarean Delivery to Facilitate Skin-to-Skin Contact.","Inclusion Criteria:\n\n* Women scheduled for elective cesarean under neuraxial anesthesia at CHU Sainte-Justine.\n* American Society of Anesthesiologists Physical Status I-III\n* Singleton pregnancy\n* Gestation ≥ 35 weeks\n* BMI \\\u003C 40\n* Able to consent in French or English\n\nExclusion Criteria:\n\n* Cesarean planned under general anesthesia.\n* Multiple pregnancy\n* Prematurity \\\u003C 35 weeks gestation\n* Major fetal anomalies\n* Morbid obesity (BMI ≥ 40)\n* Active labor\n* Emergency cesarean\n* Prisoners\n* Peripheral vascular disease requiring medication or treatment\n* Hypertensive diseases requiring medication\n* Inability to place blood pressure cuff on ankle (amputation, dysmorphism, etc.)\n* Complications requiring significant hemodynamic support (transfusions, inotropes, multiple vasopressors, etc.",{"count":59,"type":22},110,"1 Day","OBSERVATIONAL","This observational study aims to compare mean arterial pressure measurements obtained using an ankle blood pressure cuff with those obtained using a standard upper-arm cuff in pregnant individuals undergoing elective cesarean delivery under spinal anesthesia. The primary objective is to determine the level of agreement between the two measurement sites.The main question\\[s\\] it aims to answer \\[is\u002Fare\\]:\n\nDemonstrate that the mean arterial pressure is similar between arm and ankle with the blood pressure cuff\n\nEvery participant will be their own control. (Measurements will be taken at both sites on every participant)",[28,64,29,65],"Cesarean Delivery","Skin to Skin Contact",[67,68,69,70,71],"blood pressure","Mean arterial pressure","pregnancy","cesarean","skin to skin","2026-03-23",{"date":74,"type":42},"2026-03-27",{"date":76,"type":42},"2026-02-26",{"date":78,"type":22},"2026-12",{"name":80,"class":81},"St. Justine's Hospital","OTHER",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":89,"enrollmentInfo":90,"targetDuration":4,"studyType":23,"phases":92,"briefSummary":93,"conditions":94,"keywords":4,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":95,"lastUpdatePostDateStruct":96,"startDateStruct":98,"completionDateStruct":100,"leadSponsor":102,"locationsCount":50},"100617570","the-aim-of-the-study-is-to-examine-the-variation-in-blood-pressure-between-an-optimal-measurement-according-to-established-guidelines-in-the-literature---per-guidelines-and-a-common-measurement-used-by-nursing-teams---per-common-practice-among-women-of-reproductive-age-with-and-without-hyperte-100617570","NCT07320339","The Aim of the Study is to Examine the Variation in Blood Pressure Between an Optimal Measurement (According to Established Guidelines in the Literature - Per Guidelines) and a 'Common' Measurement (Used by Nursing Teams - Per Common Practice) Among Women of Reproductive Age With and Without Hyperte","Standard vs. Routine Blood Pressure Measurement in Pregnancy: Effects of Position and Diurnal Variation","Inclusion Criteria:\n\n* Women aged 18-40\n* Informed consent to participate.\n\nExclusion Criteria:\n\n* Inability to cooperate with BP measurement under optimal conditions\n* Women with complex underlying disease that may bias the data (e.g. significant vasculopathy)","40 Years",{"count":91,"type":22},500,[25],"The aim of the study is to examine the variation in blood pressure between an optimal measurement (according to established guidelines in the literature - per guidelines) and a 'common' measurement (used by nursing teams - per common practice) among women of reproductive age with and without hyperte",[29],"2025-12-21",{"date":97,"type":42},"2026-01-06",{"date":99,"type":42},"2025-08-24",{"date":101,"type":22},"2026-08-24",{"name":103,"class":49},"Hillel Yaffe Medical Center"]