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Recruiting NCT06621706

NCT06621706 Ultrasound Assessment of Gastric Volume in Diabetic Versus Non-Diabetic Term Pregnant Women Undergoing Cesarean Section

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Clinical Trial Summary
NCT ID NCT06621706
Status Recruiting
Phase
Sponsor Beni-Suef University
Condition Pulmonary Aspiration
Study Type OBSERVATIONAL
Enrollment 140 participants
Start Date 2024-09-25
Primary Completion 2025-09-25

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 40 Years
Study Type OBSERVATIONAL
Interventions
Gastric ultrasonography

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 140 participants in total. It began in 2024-09-25 with a primary completion date of 2025-09-25.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The aim of the work to compare estimated gastric volumes through ultrasound in fasting diabetic and non-diabetic pregnant women scheduled for caesarean section.

Eligibility Criteria

Inclusion Criteria: * pregnant women undergoing elective caesarean section * aged between 18-40 years * belonging to ASA II-III * gestational age greater than 37 weeks * BMI\< 35 kg/m2 Exclusion Criteria: * patients who refuse to give consent * patients taken to surgery on an emergency basis, -pregnant patients with upper gastrointestinal (GI) diseases and pathologies * patients with a history of using medications that affect gastrointestinal motility (e.g., opioids), severe organ dysfunction * pre-existing neurological deficits, intellectual disabilities and anatomical deformities.

Contact & Investigator

Central Contact

Dina M Fakhry, MD

✉ dina_fakhry_91@yahoo.com

📞 +201289998680

Principal Investigator

Dina M Fakhry, MD

PRINCIPAL INVESTIGATOR

Beni-Suef University

Frequently Asked Questions

Who can join the NCT06621706 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 40 Years, studying Pulmonary Aspiration. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06621706 currently recruiting?

Yes, NCT06621706 is actively recruiting participants. Contact the research team at dina_fakhry_91@yahoo.com for enrollment information.

Where is the NCT06621706 trial being conducted?

This trial is being conducted at Banī Suwayf, Egypt.

Who is sponsoring the NCT06621706 clinical trial?

NCT06621706 is sponsored by Beni-Suef University. The principal investigator is Dina M Fakhry, MD at Beni-Suef University. The trial plans to enroll 140 participants.

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