Prediction of Hypotension After Spinal Anesthesia in Cesarean Sections Using Non-Invasive Measurement Methods

ConditionPostspinal Hypotension

Trial statusNot yet recruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

Age18-45

SponsorIstinye University

About this trial

To compare the incidence of hypotension after spinal anesthesia and the values of perfusion index, pleth variability index, tissue oxygen saturation and tissue hemoglobin index between those who developed hypotension and those who did not develop hypotension over time.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Those who underwent elective cesarean section over the age of 18,

American Society of Anesthesia I and II,

Agree to participate in the study,

Disqualifiers

<18 or >45 years,

preeclampsia,

cardiovascular disorders,

fetal abnormalities,

Trial population

Fifty pregnant women over the age of 18 who underwent elective cesarean section, were American Society of Anesthesia I and II, and agreed to participate in the study.

Trial design

Design model

Case-crossover

Time perspective

Prospective

Treatments tested in this trial

perfusion index
Diagnostic test
To compare the incidence of hypotension after spinal anesthesia and the values of perfusion index, pleth variability index, tissue oxygen saturation and tissue hemoglobin index between those who developed hypotension and those who did not develop hypotension over time.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

tissue oxygen saturation

which indicates an increase in local tissue perfusion

Time frame

4 month

tissue hemoglobin index

indicating vasodilation

Time frame

4 month

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Istinye University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: