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Clinical Trials/CTRI/2015/08/006129
CTRI/2015/08/006129
Completed
未知

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

POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: null- PATIENTS DIAGNOSED WITH DIABETES MELLITUS (ON TREATMENT) UNDERGOING ELECTIVE SURGERYHealth Condition 2: E119- Type 2 diabetes mellitus without complications

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- PATIENTS DIAGNOSED WITH DIABETES MELLITUS (ON TREATMENT) UNDERGOING ELECTIVE SURGERYHealth Condition 2: E119- Type 2 diabetes mellitus without complications
Sponsor
POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Sponsor
POST GRADUATE INSTITUTE OF MEDICAL EDUCATION AND RESEARCH

Eligibility 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

  • •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

Outcomes

Primary Outcomes

Not specified

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