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This study is designed to assess possible relation between the anthropometric data of pregnant women at term, as well as their babies, and the maximal level of sensory blockade following spinal anesth...
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Lead Sponsor
Centre of Postgraduate Medical Education
NCT06412978 · Cesarean Delivery
NCT07244757 · Postoperative Analgesia, Cesarean Delivery, and more
NCT07102641 · Cesarean Delivery, Postpartum Comfort, and more
NCT06988982 · Spinal Anaesthesia, Spinal Anesthesia Evaluation, and more
NCT06927830 · Nausea and Vomiting, Postoperative, Cesarean Delivery, and more
Centre of Postgraduate Medical Education,Department of Anesthesia and Intensive Care
Warsaw
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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