Clinical Trials Directory

Trials / Completed

CompletedNCT06320548

The Efficacy of Preoperative Low-residue Diet on Postoperative Ileus Following Cesarean Section

The Efficacy of Preoperative Low-residue Diet on Postoperative Ileus Following Cesarean Section: A Randomized Controlled Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
166 (actual)
Sponsor
University of Roma La Sapienza · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The aim of the present study was to evaluate the efficacy of preoperative low-residue diet on postoperative ileus in women undergoing elective cesarean section. It is a surgeon-blind, randomized controlled trial enrolling pregnant women at ≥39 weeks of gestation undergoing elective cesarean section. Patients were preoperatively randomized to receive either low-residue diet (arm A) or free diet (arm B) starting from three days before surgery. The primary outcome was the postoperative ileus at 24 hours after surgery. The secondary outcomes were the postoperative pain (assessed through VAS scale), the quality of the surgical field (scored using a 5-point scale, from poor to excellent), postoperative complications, and the length of hospital stay. Perioperative data were collected and compared between groups.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTLow-residue dietPatients received clear explanations, practical schemes, and a list of allowed foods, tailored to fit individual needs.
DIETARY_SUPPLEMENTFree dietPatients had free diet.

Timeline

Start date
2018-10-01
Primary completion
2020-11-30
Completion
2020-12-02
First posted
2024-03-20
Last updated
2024-03-20

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT06320548. Inclusion in this directory is not an endorsement.