Evaluation of the Level of Oxidative Stress in Relation to the Type of Anesthesia in Parturients Whose Delivery Was Completed by Caesarean Section
NCT ID: NCT05973435
Last Updated: 2023-12-04
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
100 participants
OBSERVATIONAL
2023-03-01
2023-10-01
Brief Summary
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The main questions it aims to answer are:
* is there any association between specific parameters of pregnancy, socio-demographic characteristics and laboratory analyses with an increased level of oxidative stress
* is there any association between type of anesthesia for ceasarean section with an increased level of oxidative stress
Blood sample would be taken from the participants in the study for these analyses on three occasions in 3 test tubes (before cesarean section, during cesarean section and after cesarean section).
Researchers will compare patients that received general anesthesia with patients under spinal regional anesthesia to see if there is any difference in level of oxidative stress measured by laboratory parameters.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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General Anesthesia
Blood sampling
Blood sample would be taken from the participants in the study for these analyses on three occasions in 3 test tubes (before cesarean section, during cesarean section and after cesarean section).
Spinal anesthesia
Blood sampling
Blood sample would be taken from the participants in the study for these analyses on three occasions in 3 test tubes (before cesarean section, during cesarean section and after cesarean section).
Interventions
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Blood sampling
Blood sample would be taken from the participants in the study for these analyses on three occasions in 3 test tubes (before cesarean section, during cesarean section and after cesarean section).
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Emergency C section
18 Years
55 Years
FEMALE
Yes
Sponsors
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University Clinic Dr Dragisa Misovic-Dedinje
OTHER
Responsible Party
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Marina Boboš
Principal Investigator
Locations
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Clinical Hospital Center "Dr. Dragisa Misovic, Dedinje"
Belgrade, , Serbia
Countries
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Other Identifiers
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17/I-4
Identifier Type: -
Identifier Source: org_study_id