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Postdural Punction Headache After Ceserian Section

NCT05777694 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 750

Last updated 2023-03-21

No results posted yet for this study

Summary

The aim of this study is to compare the effect of spinal needle type on postdural puncture headache in patients who will undergo cesarean section.

The main question\[s\] it aims to answer are:

\[Does spinal needle thickness affect postdural puncture headache?\]

\[What is the response of patients who develop postdural puncture headache to treatment?\] In cases accepting cesarean section operation under spinal anesthesia, different tables were used with spinal needles, and it will be questioned whether headache will develop in the first 15 days postoperatively. Postdural puncture headache after surgery will be described.

Conditions

  • Postdural Puncture Headache
  • Regional Anesthesia Morbidity
  • Pregnancy Related

Interventions

PROCEDURE

Patients who underwent cesarean section under spinal anesthesia with 25 gauge spinal needle

the investigators performed spinal anesthesia with 25 gauge pencil point spinal needle to that patient group for prevent postdural puncture headache

PROCEDURE

Patients who underwent cesarean section under spinal anesthesia with 26 gauge spinal needle

the investigators performed spinal anesthesia with 26 gauge pencil point spinal needle to that patient group for prevent postdural puncture headache

PROCEDURE

Patients who underwent cesarean section operation under spinal anesthesia with 27 gauge spinal needle

the investigators performed spinal anesthesia with 27 gauge pencil point spinal needle to that patient group for prevent postdural puncture headache

Sponsors & Collaborators

  • Bakirkoy Dr. Sadi Konuk Research and Training Hospital

    lead OTHER_GOV

Principal Investigators

  • Duygu Akyol, M.D · Başakşehir Çam & Sakura City Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-01
Primary Completion
2022-05-01
Completion
2022-05-01

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05777694 on ClinicalTrials.gov