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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04195087
Other study ID # AntalyaEAH02
Secondary ID
Status Completed
Phase
First received
Last updated
Start date December 2, 2019
Est. completion date February 28, 2020

Study information

Verified date July 2020
Source Antalya Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date February 28, 2020
Est. primary completion date January 31, 2020
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Pregnant women who will undergo elective cesarean section

Exclusion Criteria:

- Preeclampsia

- Cardiovascular disorder

- Fetal abnormality

- Patients who failed spinal anesthesia or switched to general anesthesia during operation.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Turkey University of Health Sciences, Antalya Training and Research Hospital Antalya

Sponsors (1)

Lead Sponsor Collaborator
Antalya Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perfusion index Perfusion index will be recorded from the monitor. Before spinal anesthesia in supine positon
Primary Pleth variability index Pleth variability index will be recorded from the monitor. Before spinal anesthesia in supine positon
Primary Perfusion index Perfusion index will be recorded from the monitor. Before spinal anesthesia in sitting positon
Primary Pleth variability index Pleth variability index will be recorded from the monitor. Before spinal anesthesia in sitting positon
Primary Perfusion index Perfusion index will be recorded from the monitor. 1 minutes after spinal anesthesia in supine positon
Primary Pleth variability index Pleth variability index will be recorded from the monitor. 1 minutes after spinal anesthesia in supine positon
Primary Perfusion index Perfusion index will be recorded from the monitor. Start of the surgery
Primary Pleth variability index Pleth variability index will be recorded from the monitor. Start of the surgery
Primary Perfusion index Perfusion index will be recorded from the monitor. 1 minutes after the umbilical cord clamping
Primary Pleth variability index Pleth variability index will be recorded from the monitor. 1 minutes after the umbilical cord clamping
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