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To find out the volume and contents of stomach using ultrasonography in diabetic and non-diabetic patients posted for surgeries and finding out the relation of this with postoperative nausea and vomiting.

Assessing the fasting volume and contents of stomach using ultrasonography in diabetic and non-diabetic patients posted for elective surgery and evaluating the incidence in postoperative nausea and vomiting.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2021/02/031585
Enrollment
53
Registered
2021-02-26
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: E088- Diabetes mellitus due to underlying condition with unspecified complications

Interventions

Intervention1: gastric ultrasonography: gastric ultrasonography will be done one hour prior ro elective surgery

Sponsors

Dr LH Hiranandani hospital Powai
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: preoperative fasted patients, ASAPS class 1-3, BMI <30.

Exclusion criteria

Exclusion criteria: patient refusal, pregnant patients, BMI >30, upper GI anomaly, history of any abdominal surgery, patient with any difficult airway or difficult spinal anaesthesia.

Design outcomes

Primary

MeasureTime frame
To assess the gastric content and volume (qualitatively and quantitatively) using ultrasound in diabetics and non-diabetics posted for elective surgery. The main objective is to compare the frequency of a full stomach in the diabetic population compared to non-diabetic population. Timepoint: To compare the incidence with post operative nausea and vomitting as soon as the surgery will end.—

Secondary

MeasureTime frame
feasibility of ultrasonography as noninvasive tool in evaluating gastric contents and volume, to compare impact of duration of fasting in both diabetics and non diabetics, to determine the standard fasting guidelines if they can protect against pulmonary aspiration.Timepoint: in 24 weeks—

Countries

India

Contacts

Public ContactAnuja Nikam

Dr. L H Hiranandani hospital

dramolpradhan@gmail.com9819390204

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026