Comparision between ERAC (Enhanced Recovery after ceaserean section)Criteria and Traditional method of Recovery
- Conditions
- Pregnant Females
- Registration Number
- CTRI/2023/02/049782
- Lead Sponsor
- Aditya Singh
- Brief Summary
•Enhanced recovery after cesarean provides an evidenced based system to improve maternal based outcomes ,fuctional recovery,maternal infant bonding,and patient experience.ERAC involves multidisciplinary team efforts of anesthesiologists,obstetrician,nursing staff,hospital and patient.
•ERAC is best conceptualized as a continuum of care ,from preconception outreach,antepartum optimization,intrapartum care, which includes the anesthetic management and concluding with postpartum inpatient care and outpatient support .
•Enhanced recovery was first described by in 1997 by wilmore and kehlet.The concept was first introduced in colorectal surgeries and now practiced across all specialities
•There is wide variation in the components of enhanced recovery after surgery among different specialities but the principle remain same. The various components of Enhanced recovery includes provision of preadmission, information to expectant mothers ,Good perioperative nutrition and hydration ,minimally invasive surgical technique, efforts to maintain normothermia ,prevention of postoperative nausea and voimiting, effective peri- operative pain relief, early post operative oral intake, removal of urinary cathter,readiness to discharge and postoperative mobilization.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Female
- Target Recruitment
- 200
25 to 40 years women having gestation age more than 38 weeks posted for elective caesearean section will be included in the study.
Prior medical illness like anemia, cardiac ,renal , thyroid diseases, hypertensive disorder of pregnancy, gestational diabetes, intra and post postpartum heamorrage ,bladder injury and bowel injury will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Our primary outcome is to asses Patient satisfaction and Our primary outcome is to assess | 1) The readiness of discharge in 3rd,5th and 7th postoperative day | 2) Patient satisfaction upto 24hours postoperative in postoperative period Readiness of discharge in postoperative period Our primary outcome is to assess | 1) The readiness of discharge in 3rd,5th and 7th postoperative day | 2) Patient satisfaction upto 24hours postoperative in postoperative period
- Secondary Outcome Measures
Name Time Method Our secondary outcome is to asses 1)Post operative pain assessment 2)Requirement of post operative analgesia
Trial Locations
- Locations (1)
PDU MEDICAL COLLEGE AND CIVIL HOSPITAL
🇮🇳Rajkot, GUJARAT, India
PDU MEDICAL COLLEGE AND CIVIL HOSPITAL🇮🇳Rajkot, GUJARAT, IndiaAditya SinghPrincipal investigator9755388711timmydbz@gmail.com