Clinical Trials Directory

Trials / Completed

CompletedNCT04195087

Perfusion Index and Pleth Variability Index in Cesarean Section.

Perfusion Index and Pleth Variability Index in Predicting Hypotension Following Spinal Anesthesia Performed in Sitting Position in Cesarean Section.

Status
Completed
Phase
Study type
Observational
Enrollment
46 (actual)
Sponsor
Antalya Training and Research Hospital · Other Government
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate the predictability of hypotension by using PI and PVI in pre-and post-spinal anesthesia periods in cesarean section cases in the sitting position.

Detailed description

Spinal anesthesia has been widely used all over the world due to its superiority to general anesthesia in cesarean section. However, as a result of the sympathetic blockade in spinal anesthesia, vascular tone decreases and hypotension occurs. The incidence of hypotension increases up to 70% in pregnant women due to increased sensitivity to local anesthetics and increased intraabdominal pressure. Improper management of postspinal hypotension may lead to maternal and fetal complications. Predicting the risk of hypotension in patients undergoing spinal anesthesia may allow applications such as volume loading or prophylactic vasopressor use. The perfusion index, measured by pulse Oximeters, correlates with blood flow changes at the tip of the finger so that it can detect hypotension and thus decrease in blood flow after spinal anesthesia. Pleth variability index (PVI) is a non-invasive value found in the new generation pulse oximeters. It is a parameter used in the dynamic measurement of response to fluid therapy in intensive care units. PVI can dynamically give an idea about the fluid status of the pregnant woman. Previous studies have shown that PVI may be a marker for predicting hypotension following spinal anesthesia.

Conditions

Interventions

TypeNameDescription
DEVICEMasimo Radical-7® Pulse CO-Oximeter®The perfusion index and Pleth variability index will be recorded from the device monitor.

Timeline

Start date
2019-12-02
Primary completion
2020-01-31
Completion
2020-02-28
First posted
2019-12-11
Last updated
2020-07-09

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04195087. Inclusion in this directory is not an endorsement.