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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Low-residue diet | Patients received clear explanations, practical schemes, and a list of allowed foods, tailored to fit individual needs. |
| DIETARY_SUPPLEMENT | Free diet | Patients 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.