Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03184532
Other study ID # rec003
Secondary ID
Status Not yet recruiting
Phase N/A
First received June 9, 2017
Last updated June 9, 2017
Start date July 1, 2017
Est. completion date December 31, 2017

Study information

Verified date June 2017
Source Healthpoint Hospital
Contact Mohamed Sayed Elahl, MD
Phone 00971501257051
Email m.elahl@healthpoint.ae
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

To reduce the risk of perioperative pulmonary aspiration of gastric contents, oral intake of liquids or solids is not allowed for certain periods. Recently, the ultrasound (US) is used to evaluate the volume and the nature of the stomach content. In its latest recommendations, the American Society of Anesthesiologists (ASA) shortened the duration preoperative fasting. The aim of the study is to evaluate the efficacy of ASA recommendations in diabetic patients using ultrasound (US) scanning of the stomach (antrum).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date December 31, 2017
Est. primary completion date December 15, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients scheduled for elective orthopedic procedures.

Exclusion Criteria:

- Patients with BMI > 35 kg.m-2, age <18y, ASA physical state >II, fasting more than 6hs, or with gastric diseases will be excluded

Study Design


Related Conditions & MeSH terms

  • Evaluation of ASA Fasting Recommendations in Diabetic Patients

Intervention

Diagnostic Test:
ultrasound
ultrasound examination of pyloric antrum

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Healthpoint Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary gastric volume bedside test 5 minutes