Carotid Flow Measurements in Pregnant Women

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age20-40
SponsorHaseki Training and Research Hospital

About this trial

The goal of this observational study is to reveal the relation between carotid flow changes and post-spinal hypotension in pregnant women between the ages of 20-40. The main question it aims to answer is:

Do the carotid flow blood flow measurements and corrected flow time change before and after spinal anaesthesia related to postspinal hypotension? Participants are already receiving spinal anaesthesia to receive a caesarean section. As part of their regular anaesthesia management protocol, they will answer questions about anaesthesia management. The participants will only examined by ultrasound twice.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

"Uncomplicated term pregnant women aged 20-40 years classified as ASA 1-2.

Disqualifiers

Those diagnosed with preeclampsia or eclampsia or with systolic blood pressure above 160

Trial population

pregnant women scheduled for cesarean section

Trial design

Design model

Case-control

Time perspective

Prospective

Treatments tested in this trial

  • carotid ultrasound

    Other intervention

    The investigator will perform a carotid ultrasound just 2 cm before the carotid bulb and measure the corrected flow time and flow using Doppler and pulse wave analysis. The corrected carotid flow time will be calculated according to Bazett's equation.

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: postspinal hypotension1 intervention

Trial outcomes

Primary outcomes

1

postspinal hypotension

Hypotension is defined as (1) a decrease in systolic blood pressure \>30% or a decrease in mean arterial pressure (MAP) \>20% from baseline, or (2) systolic blood pressure \<90 mmHg or MAP \<65 mmHg.

Time frame
from spinal anaesthesia till surgical delivery

Secondary outcomes

1

fluid resuscitation

amount of fluid given for co loading during anaesthesia application

Time frame
from spinal anaesthesia till surgical delivery

Other outcomes

Sponsors and contacts

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