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
70 participants
OBSERVATIONAL
2018-07-20
2018-08-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Group G
Patients undergoing general anesthesia HSCRP and NLR measurement
HSCRP and NLR
hs-CRP levels and NLR values will be studied from routine blood samples.
Group R
Patients undergoing spinal anesthesia HSCRP and NLR measurement
HSCRP and NLR
hs-CRP levels and NLR values will be studied from routine blood samples.
Interventions
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HSCRP and NLR
hs-CRP levels and NLR values will be studied from routine blood samples.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* chronic diseases (diabetes mellitus, hypertension, heart disease, renal disease, hypo/hyperthyroidism)
* any infections,
* smoking
* contraindications for central neuraxial anesthesia.
* Pregnancies complicated with rupture of membranes, placenta previa, eclampsia/preeclampsia, and abruptio placenta
* fetal anomalies,
* abnormality detected at fetal well-being tests
18 Years
42 Years
FEMALE
No
Sponsors
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Ufuk University
OTHER
Responsible Party
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Hakan Yılmaz
Assoc Prof
Principal Investigators
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Hakan Yılmaz, MD
Role: PRINCIPAL_INVESTIGATOR
Ufuk University
Locations
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Ufuk University
Ankara, Balgat, Turkey (Türkiye)
Countries
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References
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Chen Y, Jiang S, Wu Y. Effect of 2 different anesthesia methods on stress response in neurosurgical patients with hypertension or normal: A prospective clinical trial. Medicine (Baltimore). 2016 Aug;95(35):e4769. doi: 10.1097/MD.0000000000004769.
Farzadnia M, Ayatollahi H, Hasan-Zade M, Rahimi HR. A comparative study of vascular cell adhesion molecule-1 and high-sensitive C-reactive protein in normal and preeclamptic pregnancies. Interv Med Appl Sci. 2013 Mar;5(1):26-30. doi: 10.1556/IMAS.5.2013.1.5. Epub 2013 Mar 19.
Other Identifiers
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hsCRP
Identifier Type: -
Identifier Source: org_study_id
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