Actively Recruiting
Preoperative Neutrophil-to-Lymphocyte Ratio as a Predictor of Post-Dural Puncture Headache Following Cesarean Section Under Spinal Anesthesia
Led by Istinye University · Updated on 2025-07-24
821
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are investigating whether systemic inflammatory markers, especially the neutrophil-to-lymphocyte ratio (NLR) from preoperative blood counts, can predict the development of post-dural puncture headache (PDPH) in women undergoing cesarean section with spinal anesthesia. This observational study focuses on comparing patients who develop PDPH to those who do not after this procedure. The trial is led by Istinye University and aims to improve understanding of PDPH risk factors in obstetric patients. The study observes preoperative inflammatory markers including NLR, platelet-to-lymphocyte ratio (PLR), and systemic inflammatory response index (SIRI) without administering any additional treatment or intervention. Participants are grouped based on the presence or absence of PDPH following spinal anesthesia during cesarean section. No experimental treatments are given, as the study relies on analyzing existing blood count data and medical records. Participants will be monitored for the incidence of post-dural puncture headache within 10 days after surgery. Researchers will review preoperative blood tests and postoperative medical records to assess PDPH development. The study involves collecting and analyzing data from patient records to evaluate whether inflammatory markers can serve as predictors. The total participation duration varies depending on the follow-up period after the cesarean section.
CONDITIONS
Brief Title
Neutrophil to Lymphocyte Ratio and Postdural Headache
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 18 years or older
- Underwent elective or emergency cesarean section under spinal anesthesia
- Have complete preoperative complete blood count (CBC) data available
- No known hematological or inflammatory disease
- No intraoperative complications recorded
- Medical records accessible for postoperative follow-up regarding PDPH symptoms
You will not qualify if you...
- Age under 18
- No preoperative complete blood count data available
- Presence of hematologic malignancy, active infection, autoimmune disease, or immunosuppressive therapy
- Platelet count less than 150,000/mm�b3 or INR greater than 1.5
- Incomplete or missing medical records
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 day
Participants undergo preoperative blood tests to measure inflammatory markers before cesarean section under spinal anesthesia.
1 visit (in-person)
Duration - 10 days postoperatively
Participants are monitored for the development of postdural puncture headache (PDPH) following cesarean section under spinal anesthesia.
Follow-up assessments as part of routine postoperative care
Trial Site Locations
Total: 1 location
1
Istinye Üniversity
Istanbul, Merkez Mahallesi, Turkey (Türkiye), 34250
Actively Recruiting
Research Team
I
ilke dolgun
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Published Research Related To This Trial
The Association of Systemic Immune-Inflammation Index (SII), Systemic Immune-Response Index (SIRI), and Neutrophil-to-Lymphocyte Ratio (NLR) with Cesarean Scar Pregnancy (CSP).
Refaettin Sahin, Atakan Tanacan, Hakki Serbetci...
https://pubmed.ncbi.nlm.nih.gov/38850761Reference intervals of systemic immune-inflammation index, neutrophil-to-lymphocyte ratio, lymphocyte-to-monocyte ratio, and platelet-to-lymphocyte ratio during normal pregnancy in China.
Y-Y Bai, Y Xi, B-B Yin...
https://pubmed.ncbi.nlm.nih.gov/36808350