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Clinical Trial Summary

Prevention of postspinal hypotension after spinal anesthesia for caesarian section by use of preoperative or intraoperative volume replacement. The comparison of crystalloid and colloid infusions and their timing via perfusion index and plethysmographic variability index.


Clinical Trial Description

To Prevent hypotension fluid replacement is usually used in pregnant patients scheduled for C/S. Different types of fluids can be used in order to achieve this. Also the timing of fluid replacement is important. In the present study patients were separated into 4 groups. Each receiving a one of two fluids in different times. ( Colloid pre-load, colloid co-load, crystalloid co-load and crystalloid pre-load.) The effect of overall hemodynamics and the incidence of hypotension are evaluated. Also peripheric monitors like perfusion index and plethysmographic variability index are evaluated for correlation. ;


Study Design


Related Conditions & MeSH terms

  • Complications; Anesthesia, Spinal and Epidural, in Pregnancy
  • Hypotension

NCT number NCT02680678
Study type Interventional
Source Balikesir University
Contact
Status Completed
Phase N/A
Start date April 2014
Completion date December 2016

See also
  Status Clinical Trial Phase
Completed NCT01821807 - Comparison of Two Spinal Needles Regarding Postdural Puncture Headache N/A