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Effect of early oral feeding on consequences of Cesarean section

Investigating the effect of early oral feeding on consequences and complications of elective Cesarean section

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240630062285N1
Enrollment
120
Registered
2024-07-05
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

post operative ileus. Ileus, unspecified

Interventions

Intervention 1: Intervention group: Patients who experience early oral feeding 4 hours after cesarean delivery. Patients undergo elective cesarean section in the morning. Initiation of feeding 4 hours

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Pregnant women at or beyond 37 weeks of gestation who are candidates for elective cesarean section under spinal anesthesia

Exclusion criteria

Exclusion criteria: Patients who experienced severe adhesions during their cesarean section Procedure duration was longer than 45 minutes Women with underlying gastrointestinal conditions such as inflammatory bowel disease Patients with emergency delivery indications (e.g., placenta previa, premature rupture of membranes, etc.) Patients who, for any reason, including contraindications to general anesthesia or spinal anesthesia, or personal preference, did not receive spinal anesthesia during their cesarean section Women who experienced postoperative hemorrhage

Design outcomes

Primary

MeasureTime frame
Time to pass flatus post cesarean. Timepoint: Every 6 hours until the patient experiences first flatus passage. Method of measurement: Patient self-report and documentation in the medical record.

Secondary

MeasureTime frame
Time to first bowel movement after cesarean section. Timepoint: Every 6 hours until the patient experiences first bowel movement. Method of measurement: Patient self-report and documentation in the medical record.;Maternal satisfaction with hospital stay. Timepoint: At the end of hospitalization. Method of measurement: Visual Analogue Scale.;Abdominal cramp. Timepoint: Every 6 hours throughout the hospital stay. Method of measurement: Patient self-report and physician examination using a checklist.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArian Faramarzinia

Tehran University of Medical Sciences

Arianfaramarzinia79@gmail.com+98 21 5565 8500

Outcome results

None listed

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