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Clinical Trial Summary

The aim of the study is to observe the rate of postdural puncture headache observed after spinal anesthesia in cesarean section patients.

Two kind of spinal anesthesia needles will be used:

1. 26 Gauge Quincke (cutting-tip needle)

2. 26 Gauge Atraucan (atraumatic needle)

The investigators will observe:

1. Number of spinal punctures

2. Time required for the spinal anesthesia procedure

Patients will be evaluated after 7 days for:

1. Headache

2. Backache


Clinical Trial Description

It is a known phenomenon that spinal anesthesia sometimes results in headache.

The aim of the study is to observe the rate of postdural puncture headache observed after spinal anesthesia in cesarean section patients.

Two kind of spinal anesthesia needles will be used:

1. 26 Gauge Quincke (cutting-tip needle)

2. 26 Gauge Atraucan (atraumatic needle)

We will observe:

1. Number of spinal punctures

2. Time required for the spinal anesthesia procedure

Patients will be evaluated after 7 days for:

1. Headache

2. Backache

2 kind of spinal anesthesia needles will be used, but no comparison will be made. This is an observational study. Although literature gives different rates of postdural puncture headache for these two needles, we observe the same rate of headache in our clinical practice. We want to define the real rate of postdural puncture headache in patients undergoing cesarean section with spinal anesthesia. ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT01821807
Study type Observational
Source Adiyaman University Research Hospital
Contact
Status Completed
Phase N/A
Start date June 2013
Completion date July 2013

See also
  Status Clinical Trial Phase
Completed NCT02680678 - The Effect of the Timing of Colloid and Crystalloid Infusions on Postspinal Hypotension After Spinal Anesthesia for Caesarian Section N/A