Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
124 participants
OBSERVATIONAL
2023-12-01
2024-05-31
Brief Summary
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* Can preoperative abdominal circumference predict patients with difficult spinal anesthesia
* Can preoperative abdominal circumference predict the occurrence of maternal hypotension during cesarean section Participants will be examined preoperatively in terms of visibility and palpation of spinous processes, abdominal circumference will be measured in the supine and sitting positions with other clinical parameters. Spinal anesthesia will be performed by the same experienced anesthesiologist with a standardized procedure. The number of skin punctures, needle reorientations, traumatic Cerebrospinal fluid, need for a paramedian approach or failure will be recorded. Maternal blood pressure and vasopressor requirements will also be monitored.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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Measure of abdominal circumference
Measure of abdominal circumference preoperatively in both sitting and lying position
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Umbilical cord prolapse
* Scoliosis
* Contraindication to spinal anesthesia
* Medical history of spinal surgery American Society of Anesthesia Status 4 or 5
18 Years
FEMALE
No
Sponsors
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CHU Mohammed VI Marrakech
OTHER
Responsible Party
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Meryem Essafti
Assistant Professor
Locations
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CHU Mohammed VI
Marrakesh, , Morocco
Countries
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References
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Yu C, Gu J, Liao Z, Feng S. Prediction of spinal anesthesia-induced hypotension during elective cesarean section: a systematic review of prospective observational studies. Int J Obstet Anesth. 2021 Aug;47:103175. doi: 10.1016/j.ijoa.2021.103175. Epub 2021 May 1.
Merveille OC, Childers MK, Kreimid MM, George WD. Weaning from mechanical ventilation in a general rehabilitation center: a commentary. Am J Phys Med Rehabil. 1999 Jan-Feb;78(1):85-6. doi: 10.1097/00002060-199901000-00022. No abstract available.
Provided Documents
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Document Type: Study Protocol
Document Type: Informed Consent Form
Other Identifiers
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59/2023
Identifier Type: -
Identifier Source: org_study_id
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