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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03956186
Other study ID # KSU 2019-07
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 21, 2019
Est. completion date July 11, 2019

Study information

Verified date July 2019
Source Kahramanmaras Sutcu Imam University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Spinal anesthesia for caesarean section is associated with a decrease in systemic vascular resistance and cardiac output and may cause hypotension in a significant portion of the parturients. Hypotension during delivery may cause maternal and fetal complications. If parturients who are likely to develop hypotension after spinal anesthesia can be identified before surgery, anesthesiologists would have opportunity to take measures such as prophylactic vasopressor administration. Perfusion index (PI) measured by pulse oximetry reflects vasomotor tone which affects the degree of hypotension after spinal anesthesia. This is a non-invasive method of assessing the relative vascular tone with the use of pulse oximeter which calculates the ratio of pulsatile versus the non-pulsatile component of the blood flow. A lower PI indicates greater peripheral vasomotor tone. Pleth variability index (PVI) is calculated using maximum and minimum values of perfusion index during respiratory cycles. PVI is one of the dynamic indices that can predict fluid responsiveness. There are several studies investigating the predictive value of finger PI and PVI on hypotension after spinal anesthesia. However the aortocaval compression by the gravid uterus directly effects the lower extremity perfusion. So, in this study we aimed to investigate whether the right toe PI and PVI values at supine and left lateral positions can predict hypotension during caesarean section.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date July 11, 2019
Est. primary completion date July 11, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria:

- singleton parturient

- planned for elective LSCS under spinal anesthesia

Exclusion Criteria:

- gestational age < 36 weeks

- emergency cases

- placenta previa, pre-eclampsia

- BMI>40

- Reynauld disease

- patient refusal

- cardiovascular disease

Study Design


Locations

Country Name City State
Turkey Kahramanmaras Sutcu Imam University Kahramanmaras In The USA Or Canada, Please Select...

Sponsors (1)

Lead Sponsor Collaborator
Kahramanmaras Sutcu Imam University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary pleth variability index (PVI) PVI values (%)at supine and lateral positions, before and after spinal anesthesia will be recorded and compared between the 2 groups. perioperative
Primary Perfusion index (PI) PI values(%)at supine and lateral positions, before and after spinal anesthesia will be recorded and compared between the 2 groups. perioperative
Secondary blood pressure (mmHg) blood pressure will be recorded perioperative
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