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COMPARISON OF STOMACH CONTENTS IN DIABETIC AND NORMAL PATIENTS USING ULTRASOUND

COMPARISON OF FASTING GASTRIC VOLUME IN DIABETIC AND NON-DIABETIC PATIENTS USING ULTRASOUND

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2015/08/006129
Enrollment
100
Registered
2015-08-21
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: null- PATIENTS DIAGNOSED WITH DIABETES MELLITUS (ON TREATMENT) UNDERGOING ELECTIVE SURGERY Health Condition 2: E119- Type 2 diabetes mellitus without complications

Interventions

None listed

Sponsors

POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: •Study group - Patients with diagnosed type 1 or type 2 DM on either oral hypoglycaemics or insulin therapy •Control group - Non-diabetic patients with fasting blood sugar (FBS) levels of less than 100 mg/dl or random blood sugar (RBS) levels of less than 140 mg/dl. For both groups, the standard inclusion criteria will be : •Age more than 18 years. •ASA grade I-III. •Patients posted for elective surgery before noon.

Exclusion criteria

Exclusion criteria: •Patients on medication for upper GIT symptoms. •Patients having hypothyroidism or connective tissue disease affecting GIT motility. •Patients with smoking history. •Patients on anti-depressant medication. •Previous oesophageal or abdominal surgery leading to impaired GIT function. •Patients having impaired fasting glucose or RBS levels between 140-199 mg/dl (pre-diabetes). •Morbidly obese patients with a body mass index (BMI) of more than 40. •Pregnant females. .patients with nasogstric tube in situ

Design outcomes

Primary

MeasureTime frame
The primary aim of the study is to compare the fasting gastric contents and volume using ultrasound in diabetic and non-diabetic patients undergoing elective surgery under general or regional anaesthesiaTimepoint: Patients taken up for surgery before noon prior to provision of anaesthesia .

Secondary

MeasureTime frame
The secondary aim is to validate the use of ultrasound as a non invasive bedside method to assess the gastric fluid volume.Timepoint: Patients taken up for surgery before noon prior to provision of anaesthesia.

Countries

India

Contacts

Public ContactDR HEENA GARG

PGIMER

podder_s@yahoo.co.in07087009526

Outcome results

None listed

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