Comparison of Gastric Volume in Diabetic and Non-Diabetic Pregnant Women After Preoperative Clear Fluid Intake
This study aims to compare the gastric volume, measured by ultrasonography, between diabetic and non-diabetic pregnant women after they consume clear fluids before an elective cesarean delivery.
Data Collection
Collected from today forward - ProspectiveUrogenital Diseases+6
+ Diabetes Mellitus
+ Endocrine System Diseases
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: December 1, 2025
Actual date on which the first participant was enrolled.This study focuses on understanding how drinking clear fluids before surgery might affect the stomach in pregnant women, particularly those with diabetes. The fear is that the liquid might not empty from the stomach quickly enough, leading to complications during anesthesia. Pregnancy itself can slow down stomach emptying, and diabetes might worsen this due to a condition called gastroparesis. The study aims to compare how much liquid remains in the stomach of diabetic and non-diabetic pregnant women after drinking water following standard fasting guidelines. This research is important as it could help improve the safety of anesthesia for pregnant women, especially those with diabetes. In this study, 70 pregnant women scheduled for elective cesarean delivery will participate, half of them with diabetes. All participants will drink 200 ml of water two hours before surgery. Ultrasound scans of the stomach will be taken before and after drinking the water. The scans will help determine the amount of liquid in the stomach and its consistency. The primary goal is to compare the stomach volume between diabetic and non-diabetic pregnant women. The study will also assess the risk of liquid entering the lungs during anesthesia, which is defined as a stomach volume greater than 1.5 ml/kg.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.70 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Female
Biological sex of participants that are eligible to enroll.From 18 to 40 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Ankara Bilkent City Hospital
Ankara, Turkey (Türkiye)Open Ankara Bilkent City Hospital in Google Maps