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Prediction of Postdural Puncture Headache

Recruitingn/aAges 18 Years - 45 YearsFemaleAmasya University
NCT07706751 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

The primary objective of this study is to evaluate the effectiveness of inflammation index (pan-immune inflammation value, systemic immune inflammation index, and systemic inflammatory response index) values, calculated from routine pre- and post-operative blood test (hemogram) results of pregnant women undergoing cesarean section under spinal anesthesia, in predicting postdural puncture headache. Significant results will allow for the early identification of the population at risk of developing PPH and the implementation of preventive measures. The secondary objectives of the study are to evaluate the effects of factors such as demographic data (age, height, weight, and body mass index) obtained from patient records and the hospital information system, number of births, blood group, infant birth weight, smoking, previous history of postdural puncture headache (PPH), or headache in gener

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📋 Eligibility rules (as published)
Inclusion Criteria: * . Pregnant women who are of a cognitive level capable of giving informed consent * Pregnant women aged 18-45 who have undergone elective cesarean section * Term (37 weeks and above) pregnant women * Patients with an American Society of Anesthesiologists (ASA) physical status score of 2 (ASA II) Exclusion Criteria: * History of active infection or chronic inflammatory disease * History of steroid or immunomodulatory drug use * Presence of coagulopathy or hematological disorder * Presence of preeclampsia/HELLP syndrome * Those who received blood transfusions during and after surgery
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What it tests

  • Not listed
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Where

1 site
Amasya University Training and Research Hospital
Amasya, Turkey (Türkiye)
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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