Observational study in patients undergoing gynaecological surgeries to estimate the duration of perioperative fasting and its effect on the recovery profile.
Not Applicable
- Conditions
- Health Condition 1: N72- Inflammatory disease of cervix uteriHealth Condition 2: N889- Noninflammatory disorder of cervixuteri, unspecified
- Registration Number
- CTRI/2024/05/067885
- Lead Sponsor
- Other
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing elective gynaecological and Gynaecologic oncology surgeries.
Age group 18 to 65
ASA 1 &2
Exclusion Criteria
ASA 3 and 4 patients
emergency surgeries
Surgery needing massive blood transfusion
Surgeries with elective/unanticipated post op ventilation
Surgeries requiring post op ICU admission.
Age less than 18 years and more than 65 years
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of hours of preoperative and postoperative fastingTimepoint: postoperatively
- Secondary Outcome Measures
Name Time Method To determine the effect of hours of fasting and time for <br/ ><br>resumption of fasting on recovery profile including postoperative nausea and <br/ ><br>vomiting, ambulation, pain scores, number of days in hospital. To identify risk factors <br/ ><br>for prolonged perioperative fasting in gynaecological surgeries.Timepoint: 24hours