Effect of Anesthesia Method on Neutrophil-Lymphocyte Ratio
The Effect of Anesthesia Method on Neutrophil-Lymphocyte Ratio in Patients Undergoing Forearm Surgery
1 other identifier
observational
1
1 country
1
Brief Summary
The neutrophil/lymphocyte ratio (NLR) is a simple and inexpensive marker of the inflammatory response. NLR is affected not only by surgical trauma but also by the anesthetic method. The method of anesthesia can affect NLR, thereby modulating the inflammatory response and surgical outcomes. In this study, it was aimed to evaluate the relationship between blood NLR and anesthesia techniques in patients undergoing forearm surgery, and the secondary aim was to evaluate the relationship between Platelet/lymphocyte ratio (TLR), Mean Platelet Volume (MPV) and anesthesia techniques.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jan 2018
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 2021
CompletedFirst Submitted
Initial submission to the registry
November 17, 2022
CompletedFirst Posted
Study publicly available on registry
November 29, 2022
CompletedNovember 29, 2022
November 1, 2022
2.8 years
November 17, 2022
November 28, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Neutrophil/lymphocyte ratio
Differences in neutrophil-lymphocyte ratio between patients who underwent general anesthesia and peripheral nerve block
up to 24 hours after surgery
Secondary Outcomes (2)
Platelet/lymphocyte ratio
up to 24 hours after surgery
Mean Platelet Volume
up to 24 hours after surgery
Study Arms (2)
Group G
Patients Undergoing Forearm Surgery under general anesthesia
Group P
Patients Undergoing Forearm Surgery under peripheral nerve block
Interventions
Eligibility Criteria
Patients aged 18-65 years who have underwent forearm surgery
You may qualify if:
- Underwent forearm surgery
- Between aged 18-70
- Under general anesthesia or peripheral nerve block
You may not qualify if:
- acute infection
- morbid obesity
- chronic treatment with steroids or immunosuppressants
- recently received chemotherapy
- hepatic and renal dysfunction;
- chronic alcohol abusers
- Multiple trauma
- Patients with missing data in their files
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Zonguldak Bülent Ecevit University Medicine Faculty
Zonguldak, Kozlu, 67600, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- medical doctor
Study Record Dates
First Submitted
November 17, 2022
First Posted
November 29, 2022
Study Start
January 1, 2018
Primary Completion
November 1, 2020
Study Completion
November 1, 2021
Last Updated
November 29, 2022
Record last verified: 2022-11
Data Sharing
- IPD Sharing
- Will not share