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Early Oral Intake Following Cesarean Surgery

Early Oral Intake Following Elective Cesarean Surgery in Iranian Women; the Economic Burdens and Patient Satisfaction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00370708
Enrollment
Unknown
Registered
2006-09-01
Start date
2003-04-30
Completion date
2004-02-29
Last updated
2006-09-07

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

Conditions

Obstetrics, Surgery

Keywords

Cesarean, Oral, Intake

Brief summary

In this study we are trying to compare the safety and financial benefit of starting the realimentation early versus conventional oral intake following the Cesarean surgery in Iran.

Detailed description

Cesarean delivery is announced to constitute 50% of deliveries in the Capital and 39% of all the deliveries nationwide, which is far beyond the acceptable international normal range, according to the official site of the Ministry of Health and Medical Education of the Islamic Republic of Iran \[http://www.mohme.gov.ir/HNDC/Indicators/Simaye\_Salamt/Simaye\_Salamat.htm\]. This high rate of elective cesarean deliveries might be due to several reasons which are far beyond the scope of this study. Here we tried to see whether the reduction in the time of hospitalization for these patients is safe at the expense of earlier oral realimentation and to see whether this strategy increases the patients' satisfaction or not.

Interventions

PROCEDUREOral Intake following admittance to the postpartum ward

Sponsors

Tehran University of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Women who had elective cesarean deliveries under regional anesthesia

Exclusion criteria

1. Receiving general anesthesia, magnesium sulfate or insulin. 2. Coming across an intraoperative bowel injury. 3. Having any medical or gastrointestinal problem that prohibits early feeding

Design outcomes

Primary

MeasureTime frame
Tolerance of Oral Intake

Countries

Iran

Outcome results

None listed

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