The Effect of General and Spinal Anesthesia on Neutrophil-to-lymphocyte Ratio
NCT ID: NCT05409885
Last Updated: 2022-07-21
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
60 participants
OBSERVATIONAL
2022-03-20
2022-07-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effect of Injection Rate of Local Anesthetic in Caesarean Section
NCT05091294
Neutrophil to Lymphocyte Ratio and Postdural Headache
NCT07075874
Does Smoking Effect Spinal Anesthesia?
NCT05343845
The Effect of Combined Spinal Epidural Anaesthesia on QTc Interval Undergoing Cesarean Section
NCT06018805
Can Passive Leg Raise Prevent Spinal Anesthesia-induced Hypotension During Cesarean Section?
NCT04673253
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The primary endpoint was to compare the effects of general and spinal anesthesia on umbilical cord NLR. Secondary endpoints were determined the general and spinal anesthesia on routine umbilical cord PLR, MPV and newborn Apgar scores at 1st and 5th min.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_CONTROL
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
General anesthesia group
Evaluate the effects of general anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
General anesthesia
Evaluate the effects of general anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
Spinal anesthesia group
Evaluate the effects of spinal anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
Spinal anesthesia
Evaluate the effects of spinal anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
General anesthesia
Evaluate the effects of general anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
Spinal anesthesia
Evaluate the effects of spinal anesthesia on NLR, PLR and MPV in patients undergoing cesarean section.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* American Society of Anesthesiology (ASA) II-III
* elective ceserean surgery
Exclusion Criteria
* under 18 years of age or over 45 years of age
* factors affecting NLR, PLR and MPV such as preeclampsia, HELLP syndrome or premature rupture of membranes
* history of neurological and/or neuromucular disease
* cooperation cannot be established
* emergency surgery
18 Years
45 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Antalya Training and Research Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Kerem İnanoğlu
Role: PRINCIPAL_INVESTIGATOR
Antalya TRH
Esra Bağ
Role: PRINCIPAL_INVESTIGATOR
Antalya TRH
Arzu Karaveli
Role: STUDY_DIRECTOR
Antalya TRH
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Antalya Training and Research Hospital, Department of Anesthesiology and Reanimation
Antalya, , Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
5/4
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.