Actively Recruiting

Age: 18Years - 45Years
FEMALE
NCT06434870

Effect of Spinal Anesthesia in Elective Cesarean Cases on Frontal QRS Angle in Anemic and Non-Anemic Patients

Led by Sanliurfa Mehmet Akif Inan Education and Research Hospital · Updated on 2024-05-30

100

Participants Needed

1

Research Sites

19 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The QRS-T angle represents a novel marker of myocardial repolarisation. It is defined as the angle difference between the direction of ventricular depolarisation (QRS wave) and the direction of ventricular repolarisation (T wave). It is an indicator of instability in the electrophysiological properties of the myocardium and is associated with arrhythmias. The frontal QRS-T angle is a straightforward, cost-effective parameter that can be readily obtained from 12-lead electrocardiography. The most prevalent arrhythmias during pregnancy are atrial arrhythmias. However, ventricular tachyarrhythmias are exceedingly rare during pregnancy and may be life-threatening. Caesarean section is one of the most common surgical procedures. General anaesthesia, spinal anaesthesia and epidural anaesthesia can be employed in these patients. Spinal anaesthesia is a frequently employed method in caesarean section operations due to its rapid onset of effect, technical simplicity of application and higher probability of success. In pregnant women, anaemia is defined as a haemoglobin concentration below 11 mg/dL in the first trimester, 11 mg/dL in the second trimester and 10.5 mg/dL in the third trimester.

CONDITIONS

Official Title

Effect of Spinal Anesthesia in Elective Cesarean Cases on Frontal QRS Angle in Anemic and Non-Anemic Patients

Who Can Participate

Age: 18Years - 45Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Aged 18-45 years
  • Patients with American Society of Anesthesiologists (ASA) II classification
Not Eligible

You will not qualify if you...

  • Patients with rhythm disorders
  • Patients with electrolyte disturbances
  • Patients with liver and/or renal failure
  • Obese patients (body mass index > 30)
  • Trauma patients
  • Cancer patients
  • ASA III-IV patients
  • Patients who do not wish to participate in the study will be excluded.

AI-Screening

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Trial Site Locations

Total: 1 location

1

University of Health Science Turkey Sanliurfa Mehmet Akif Inan Training and Research Hospital

Sanliurfa, Turkey (Türkiye), 63050

Actively Recruiting

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Research Team

A

ahmet kaya

CONTACT

M

mahmut alp karahan

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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