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Post Operative Feeding After Cesarean Section

A Randomized Controlled Study of Early Versus Delayed Oral Post Operative Feeding After Cesarean Section

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04338737
Enrollment
300
Registered
2020-04-08
Start date
2020-06-30
Completion date
2021-04-30
Last updated
2020-04-08

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

Conditions

Feeding Patterns

Keywords

early feeding ,late feeding

Brief summary

3 different post ceseraen secton feeding regmen are compared

Detailed description

300 women admitted to the labor and delivery unit in kasr Elainy teaching hospital, Following the decision to perform a cesarean section because of obstetric indications. The study involved only elective cesarean sections. The 300 patients participated in this work and will be randomly and equally divided into three groups: 1. Group A : It consists of 100 patients that will be allocated for early post-operative oral feeding receiving water and clear fluid approximately 2 hours after surgery, followed by soft food and regular diet 4 hours later irrespective to intestinal sounds, flatus or stool. 2. Group B : It consists of 100 patients that will be allocated for early Postoperative oral feeding receiving water and clear fluid approximately 2 hours after surgery till the return of intestinal sounds, then soft food and regular diet later on. 3. Group C : It consists of 100 patients that will receive no oral feeding till passage of flatus instead 2 to 3 Litres of intravenous fluid will be used for feeding. Water and fluid will be then offered, followed by soft foods and then a regular diet.

Interventions

OTHERtimming of feeding

post-operative oral feeding receiving water and clear fluid after surgery, followed by soft food and regular diet

Sponsors

Kasr El Aini Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Maternal age from 20 to 40. * Primigravida and previous 1 or two cesarean section. * Elective cesarean section. * Regional anaesthesia. * Singleton pregnancy

Exclusion criteria

* Medical disorders as (sever preeclampsia, diabetes, liver or kidney diseases). * Intraoperative intestinal injury. * Previous major abdominal surgery except cesarean section. * Obstructed labor with

Design outcomes

Primary

MeasureTime frameDescription
duration minutes till return of bowel soundtime interval in minutes from the end of surgery till the return of intestinal soundhearing of intestinal sound
maternal satisfaction from time of initiation of oral feeding after caesarean section.before discharge from hospital (range of 24 hours)Assessment of patient satisfaction before discharge from hospital using visual analogue scale.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026