Efficacy of early postoperative oral feeding in mothers undergoing caesarean section in Himachal Pradesh
Not Applicable
- Conditions
- Health Condition 1: O899- Complication of anesthesia duringthe puerperium, unspecified
- Registration Number
- CTRI/2023/07/054589
- Lead Sponsor
- Prarthana Jain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Elective lower segment caesarean section
2.Under subarachnoid block
3.Age 18 to 35 years
4.Singleton pregnancy
5.more than or equal to 37 weeks period of gestation
6.Participants who give consent
Exclusion Criteria
1.Non consenting participant
2.Emergency caesarean section
3.Intraoperative and postoperative complications such as gastrointestinal injury, genitourinary tract injury, and postpartum hemorrhage
4.Duration of surgery more than 60 mins
5.Previous LSCS
6.Previous history of bowel injury or surgery
7.Patients having any comorbidity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To check the efficacy & safety of early oral feeding for early recovery of bowel functions as a part of ERAS CD guidelines in parturients undergoing elective lower segment caesarean section under subarachnoid block.Timepoint: 48hrs
- Secondary Outcome Measures
Name Time Method To detect any post operative complication & check maternal satisfaction, overall & in terms of hunger & thirst after provision of early oral intake in postoperative period in Elective LSCS parturientTimepoint: study duration 10 months for research 2 months for analysis