Evaluation of the Effect of Body Mass Index on Gastric Volume With Ultrasound in Term Pregnant Women
NCT ID: NCT03555604
Last Updated: 2019-07-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
42 participants
OBSERVATIONAL
2018-05-29
2019-06-15
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ultrasound Assessment of Gastric Volume in High-Risk Pregnant Women At Term
NCT06803225
Ultrasound Assessment of Gastric Content in Fasted Pregnant Women
NCT04277013
Intra- and Interrater Reliability of Quantitative Ultrasound Assessment of Gastric Content in Term Parturients Before Elective Caesarean Delivery
NCT05946447
Quantitative Ultrasound Assessment of Gastric Volume in Pregnant Women at Term
NCT01980108
Gastric Sonography in the Fasted Term Pregnant Patient for Elective Cesarean Delivery
NCT01980121
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
CSA =(π x mean anteroposterior diameter x mean longitudinal diameter)/4
In addition to qualitative and quantitative ultrasound measures, the investigators will record demographic variables including age, BMI, weeks of gestation, gravity and parity.
The investigators plan to evaluate the existence of a relationship between cross-sectional area of the antrum (CSA) and BMI in term pregnant women using measurements of the CSA taken with free tracing calipers in ultrasound
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Scheduled cesarean section
Gastric ultrasound in term pregnant patients to correlate with NPO time in relation to body mass index
Gastric ultrasound
Gastric ultrasound to measure antrum cross sectional area
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Gastric ultrasound
Gastric ultrasound to measure antrum cross sectional area
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Age older than 18 years
3. NPO status \>6 hours
Exclusion Criteria
2. Diagnosis of upper gastrointestinal disease
3. Episode of vomiting within the last 6 hours
4. Patients taking gastric pro-kinetic medications
5. Diabetes mellitus
6. Prior gastric, esophageal or upper abdominal surgery
7. Allergy to US gel
18 Years
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Augusta University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Efrain Riveros Perez, MD
Assistant Professor Department of Anesthesiology and Perioperative Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Augusta University
Augusta, Georgia, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1184342
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.