Prediction of Postdural Puncture Headache

Sponsor
Amasya University
Study ID
NCT07706751
Status
Recruiting
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Conditions

  • Headache After Spinal Puncture
  • Pregnancy

Eligibility Criteria

Sex
FEMALE
Age
18 Years - 45 Years
Healthy Volunteers
Not accepted

Study Details

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 general, on the development of postdural puncture headache (PPH), to determine the frequency of PPH, and to identify the symptoms accompanying PPH.

Key Dates

First listed
Jul 16, 2026
Start date
Jun 15, 2026
Status verified
Jul 2026
Primary completion
Nov 15, 2026
Completion
Dec 15, 2026

Study Design

Enrollment
260 participants (estimated)

Arms

  • Arm: Patients with postdural puncture headache
    Patients with postdural puncture headache after cesarean section
  • Arm: Patients without postdural puncture headache
    Patients without postdural puncture headache after cesarean section

Primary Outcome Measure

The predictive role of inflammation indices for postdural puncture headache. [ Time Frame: 5 days ]

Central Contacts

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