Comparision of ERAS protocols versus conventional surgical protocols in gynecological surgeries
Phase 3
- Conditions
- Health Condition 1: O- Medical and SurgicalHealth Condition 2: N80-N98- Noninflammatory disorders of female genital tract
- Registration Number
- CTRI/2024/03/064314
- Lead Sponsor
- Rajendra Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing gynecological surgeries including total abdominal hysterectomy, vaginal hysterectomy, cystectomy, myomectomy.
Exclusion Criteria
Obese class 2 and diabetic patients.
Patients unwilling to participate in ERAS protocol.
Patients admitted in ICU post operatively.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Effectiveness of ERAS protocols in rate of complications post operatively.Timepoint: 4 days post operatively.
- Secondary Outcome Measures
Name Time Method Reducing post operative complications.Timepoint: 10 days