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Efficacy of early postoperative oral feeding in mothers undergoing caesarean section in Himachal Pradesh

Efficacy of early postoperative oral feeding on early recovery in parturients undergoing elective caesarean section in Himachal Pradesh: A randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/07/054589
Enrollment
154
Registered
2023-07-03
Start date
Unknown
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O899- Complication of anesthesia duringthe puerperium, unspecified

Interventions

Intervention1: Early postoperative oral feeding after 6 hrs of surgery and monitoring for 48 hrs after surgery: early postoperative oral feeding in step up approach after caesarean section after 6 hrs

Sponsors

Prarthana Jain
Lead Sponsor

Eligibility

Inclusion criteria

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

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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—

Countries

India

Contacts

Public ContactDr Prarthana Jain

Dr radhakrishnan government medical college hamirpur himachal pradesh

drmanjitkanwar@gmail.com9418731978

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026