Actively Recruiting
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
Eligibility Criteria
You may qualify if you...
- Aged 18-45 years
- Patients with American Society of Anesthesiologists (ASA) II classification
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
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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