[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"obstetric-labor\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:obstetric-labor":26},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,46,69],{"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":27,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":42,"locationsCount":45},"100649998","carbohydrate-optimized-nutritional-solution-versus-electrolyte-hydration-in-labor-100649998",false,"NCT07742748","Carbohydrate-Optimized Nutritional Solution Versus Electrolyte Hydration in Labor","Pilot Randomized Controlled Trial Evaluating Carbohydrate-Optimized Nutritional Solution Versus Electrolyte Hydration in Active Labor With Epidural Analgesia in Low-Risk Pregnant Women","Inclusion Criteria:\n\n* Pregnancy classified as Normal Pregnancy, Low-Risk Pregnancy, or Medium-Risk Pregnancy according to the \"Protocol de seguiment de l'embaràs a Catalunya\" and \"Protocol de naixement i acompanyament al naixement de Catalunya\".\n* Use of epidural analgesia during labor.\n* Ability to understand Catalan and\u002For Spanish.\n* Term pregnancy (≥37 weeks gestation).\n* Cephalic presentation.\n* Spontaneous onset of labor, OR induced labor due to prolonged pregnancy or premature rupture of membranes (regardless of duration).\n* Prenatal care at ASSIR Terres de l'Ebre with planned delivery at Hospital Universitari Tortosa Verge de la Cinta.\n* Signed informed consent prior to labor.\n\nExclusion Criteria:\n\n* Gestational diabetes (including diet and exercise controlled).\n* Multiple gestation.\n* Labor not documented in partograph.\n* Informed consent not signed prior to labor.\n* Medical indication requiring administration of glucose or glucose-saline intravenous solution during labor (withdrawal criterion).","FEMALE","18 Years",{"count":19,"type":20},147,"ESTIMATED","INTERVENTIONAL",[23],"NA","This is a pilot randomized, triple-blind clinical trial (pilot RCT) evaluating the preliminary effects of energy supplementation with carbohydrate-rich sports gels compared to a low-sugar sports drink during labor in low-risk pregnant women receiving epidural analgesia.\n\nLabor is associated with substantially increased metabolic demands, while current evidence on intrapartum carbohydrate supplementation remains heterogeneous. This study investigates whether a carbohidrate solution formulation containing improves maternal and neonatal outcomes compared to an other.\n\nA total of 142 term, low-risk pregnant women will be recruited at a single hospital center and randomized to receive either the sports gel or the control beverage. The intervention will begin 60 minutes after epidural analgesia and be repeated every 3 hours until delivery, with a maximum of 4 units administered per participant.\n\nThe primary objective is to obtain preliminary estimates of the intervention effects on labor duration and obstetric and neonatal outcomes. Secondary outcomes include cardiotocography patterns, maternal and neonatal glucose levels, postpartum hemorrhage, vomiting episodes, and maternal satisfaction.\n\nThis trial was prospectively registered. The study was initially conceived as a pilot randomized controlled trial within an institutional research framework, and registration was completed after participant recruitment had been completed to ensure transparency and adherence to international reporting standards.\n\nThe results of this pilot study will inform the design of a future large-scale randomized controlled trial.",[26],"Obstetric Labor",[28,29,30,31,32,33],"Maternal Outcomes","Labor Outcomes","Epidural Analgesia","oral carbohydrate supplementation","Dietary Supplements","maternal energy intake","RECRUITING","2026-08-01",{"date":37,"type":38},"2026-08-04","ACTUAL",{"date":40,"type":38},"2025-09-01",{"date":35,"type":20},{"name":43,"class":44},"Institut Investigacio Sanitaria Pere Virgili","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":53,"sex":54,"minAge":4,"maxAge":4,"enrollmentInfo":55,"targetDuration":4,"studyType":57,"phases":4,"briefSummary":58,"conditions":59,"keywords":4,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":45},"100474871","improvings-implementing-a-protocol-to-improve-intrapartum-sonography-skills-100474871","NCT05463536","Improvings: Implementing a Protocol to Improve Intrapartum Sonography Skills.","IMPROVINgSS","Inclusion Criteria:\n\n* Obstetric caregivers, willing to participate in the study (to give written informed consent).\n\nExclusion Criteria:\n\n* Trainees refusing to participate (refusing to give written informed consent).",true,"ALL",{"count":56,"type":20},20,"OBSERVATIONAL","Prospective observational cohort study on the learning curve for the sonographic assessment of labor progress (fetal head position and station) amongst obstetric caregivers.\n\nStudy participants: convenience sample of 20 obstetric caregivers working in the department of obstetrics and gynecology at the University Hospital of Leuven - recruited over a 12-month period.\n\nFormat of the training program:\n\n1. Observational phase: the goal is to measure the accuracy of the clinical assessment of fetal head position and station throughout the different stages of labor by caregivers working within the department.\n2. Self-study: reading of the 2018 practice guidelines on intra-partum ultrasound by ISUOG and watching the corresponding teaching video.\n3. Supervised implementation phase: one-to-one teaching by experienced sonographers, who initially demonstrate, later interactively supervise the quality of the scans acquired by the obstetric caregiver.\n4. Proficiency testing: from this point onwards, the trainee independently performs ultrasound scans in labor to asses fetal head position and station. The scans will be repeated by the expert sonographer, the results will be compared (qualitatively and quantitatively) and immediate feedback provided if indicated. Every observation will have a binary outcome (success or failure of trainee acquisition) according to predefined quality assessment criteria. Observations will be continued until proficiency is reached (saturation of the learning curve).",[26],"2024-07-01",{"date":62,"type":38},"2024-07-03",{"date":64,"type":38},"2022-07-07",{"date":66,"type":20},"2025-12-30",{"name":68,"class":44},"Universitaire Ziekenhuizen KU Leuven",{"id":70,"slug":71,"hasResults":11,"nctId":72,"briefTitle":73,"officialTitle":74,"acronym":4,"eligibilityCriteria":75,"healthyVolunteers":11,"sex":16,"minAge":76,"maxAge":4,"enrollmentInfo":77,"targetDuration":4,"studyType":21,"phases":79,"briefSummary":81,"conditions":82,"keywords":83,"overallStatus":87,"whyStopped":4,"lastUpdateSubmitDate":88,"lastUpdatePostDateStruct":89,"startDateStruct":91,"completionDateStruct":93,"leadSponsor":95,"locationsCount":4},"100552372","phase-4-multicenter-study-of-chloroprocaine-versus-ropivacaine-for-epidural-labor-analgesia-100552372","NCT06472232","Multicenter Study of Chloroprocaine Versus Ropivacaine for Epidural Labor Analgesia","Efficacy and Safety of Chloroprocaine Versus Ropivacaine for Epidural Labor Analgesia Study: a Randomized, Double-blind, Controlled, Multicenter, Noninferiority Clinical Trial","Inclusion Criteria:\n\n* Primigravid women with full-term pregnancies scheduled for labor analgesia\n* Determination of labor onset to cervical dilatation ≤ 5cm;\n* Visual analogue scale (VAS) pain score during contractions \\>50 mm (0 mm = no pain at all, 100 mm = most intense pain);\n* Age ≥20 years;\n* American Society of Anesthesiologists (ASA) classification II\n* Body mass index (BMI) between 18.5 and 30 kg\u002Fm2\n* Height \\>155 cm\n* Signed informed consent.\n\nExclusion Criteria:\n\n* Twin or multiple pregnancies\n* Hypertension\n* Severe cardiopulmonary and hepatic or renal disease\n* Severe pregnancy comorbidities such as preeclampsia, eclampsia, HELLP syndrome, placenta praevia, placental abruption, etc.\n* Cephalopelvic disproportion\n* History of allergy to local anesthesia\n* Spinal deformity\n* Contraindications to intrathecal anesthesia\n* Refusal to participate in the stud","20 Years",{"count":78,"type":20},356,[80],"PHASE4","Women requiring epidural labor analgesia were randomized into two groups, one with the local anesthetic chloroprocaine and the other with ropivacaine. The primary outcome was to observe the analgesic scores of the two groups of drugs as well as adverse reactions.",[26],[84,85,86],"labor analgesia","Chloroprocaine","Ropivacaine","NOT_YET_RECRUITING","2024-06-21",{"date":90,"type":38},"2024-06-25",{"date":92,"type":20},"2024-06-18",{"date":94,"type":20},"2025-09-30",{"name":96,"class":44},"Women's Hospital School Of Medicine Zhejiang University"]