Early Versus Delayed Oral Liquids and Soft Food After Elective Ceasarean Section

February 16, 2022 updated by: Ain Shams University
To compare the safety of early versus delayed oral feeding after uncomplicated cesarean section under spinal anesthesia

Study Overview

Detailed Description

Cesarean section is one of most common surgical procedures saving both for mother and newborn when medically indicated .traditionally patients are not given fluids or food afer abdominal surgery until bowel function return as evidenced by bowel sounds passage of flatus or stool or feeling of hunger the rationale of this practice is to prevent postoperative nausea , vomiting, distension and other complications

Study Type

Observational

Enrollment (Anticipated)

150

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Magdy Kolib
  • Phone Number: 01200520050

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

17 years to 50 years (Child, Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Women in child bearing period

Description

Inclusion Criteria:

  • previous 1,2,3 cs Uncomplicated elective cs Singletone pregnancy Spinal anesthesia

Exclusion Criteria:

  • women with medical disorder HTN, DM History of bowel surgery or intraoprative complication Contraindication to spinal anesthesia

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Group A
Early feeding group
Early versus delayed oral liquid feeding after ceasarean section
Group B
Delayed feeding group

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Time of passage of flatus
Time Frame: 6 hrs
6 hrs

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

February 20, 2022

Primary Completion (Anticipated)

March 15, 2022

Study Completion (Anticipated)

April 15, 2022

Study Registration Dates

First Submitted

January 1, 2022

First Submitted That Met QC Criteria

February 5, 2022

First Posted (Actual)

February 10, 2022

Study Record Updates

Last Update Posted (Actual)

February 18, 2022

Last Update Submitted That Met QC Criteria

February 16, 2022

Last Verified

December 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Oral feeding after ceasarean

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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