A study on Fasting and Surgery Timing
Not Applicable
- Conditions
- Health Condition 1: Z00-Z99- Factors influencing health status and contact with health servicesHealth Condition 2: O- Medical and SurgicalHealth Condition 3: O- Medical and Surgical
- Registration Number
- CTRI/2022/09/045600
- Lead Sponsor
- Mario Victor Newton
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients admitted for elective surgery.
(Operations were defined using the NCEPOD classification of surgical intervention. Elective operations were defined as intervention planned or booked in advance of routine admission to hospital. Timing tosuit patient, hospital and staff.)
Exclusion Criteria
Emergency cases, cases planned under local anesthesia, Diabetics, Chronic Liver Disease
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To conduct a Randomised Control Trial among Elective Surgery patients to assess the perioperative outcomes of reduction in preoperative fasting time with Carbohydrate loading, in terms of Peri-operative hemodynamic events, fatigue, thirst, anxiety, hunger, nausea, handgrip strength, Urine Ketone bodies, hypoglycemia.Timepoint: Baseline
- Secondary Outcome Measures
Name Time Method Intraoperative hemodynamic events like tachycarida, hypotension, need for fluid bolus, need for inotrope support, oliguria, any adverse cardiovascular events will be noted. <br/ ><br>Same will be monitored from the patient chart in the post operative period for first 48 hours.Timepoint: Intraoperative - when the patient is inside operation theatre <br/ ><br>Post operative - first 48 hours after surgery in the ward