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Comparison of Gastric Volume in Diabetic and Non-Diabetic Pregnant Women After Preoperative Clear Fluid Intake

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Study Aim

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.

What is being collected

Data Collection

Collected from today forward - Prospective
Who is being recruted

Urogenital Diseases+6

+ Diabetes Mellitus

+ Endocrine System Diseases

From 18 to 40 Years
+12 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Cohort

Tracking disease incidence in order to identify risk factors and understand disease progression over time.
Observational
Study Start: December 2025
See protocol details

Summary

Principal SponsorAnkara City Hospital Bilkent
Study Contactİrem Dinçer, MD
Last updated: March 20, 2026
Sourced from a government-validated database.Claim as a partner

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.

Official TitleEffect of Preoperative Clear Fluid Intake on Gastric Volume in Diabetic and Non-Diabetic Pregnant Women Assessed by Gastric Ultrasonography
Principal SponsorAnkara City Hospital Bilkent
Study Contactİrem Dinçer, MD
Last updated: March 20, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

70 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Cohort

These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.

Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

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

Urogenital DiseasesDiabetes MellitusEndocrine System DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsMetabolic DiseasesNutritional and Metabolic DiseasesPregnancy ComplicationsDiabetes, GestationalGlucose Metabolism Disorders

Criteria

5 inclusion criteria required to participate
ASA physical status II

Pregnant women aged 18-40 years

Singleton pregnancy

Scheduled for elective cesarean section under spinal anesthesia

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7 exclusion criteria prevent from participating
Severe systemic disease (ASA III or higher)

Known allergy to study medications

Pre-existing neurological disease

Refusal to participate in the study

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Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Study Objectives

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

Recruiting

Ankara Bilkent City Hospital

Ankara, Turkey (Türkiye)Open Ankara Bilkent City Hospital in Google Maps
Recruiting
One Study Center
Comparison of Gastric Volume in Diabetic and Non-Diabetic Pregnant Women After Preoperative Clear Fluid Intake | PatLynk