Early Versus Delayed Oral Liquids and Soft Food After Elective Ceasarean Section
Sponsor
Ain Shams University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05233280
Collaborator
(none)
150
1.8
Study Details
Study Description
Brief Summary
To compare the safety of early versus delayed oral feeding after uncomplicated cesarean section under spinal anesthesia
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
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 Design
Study Type:
Observational
Anticipated Enrollment
:
150 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Early Versus Delayed Oral Liquids and Soft Food After Elective Ceasarean Section
Anticipated Study Start Date
:
Feb 20, 2022
Anticipated Primary Completion Date
:
Mar 15, 2022
Anticipated Study Completion Date
:
Apr 15, 2022
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Group A Early feeding group |
Other: Oral liquids and soft food 2 hours postoperative
Early versus delayed oral liquid feeding after ceasarean section
|
| Group B Delayed feeding group |
Outcome Measures
Primary Outcome Measures
- Time of passage of flatus [6 hrs]
Eligibility Criteria
Criteria
Ages Eligible for Study:
17 Years
to 50 Years
Sexes Eligible for Study:
Female
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
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Ain Shams University
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Ain Shams University
ClinicalTrials.gov Identifier:
NCT05233280
Other Study ID Numbers:
- Oral feeding after ceasarean
First Posted:
Feb 10, 2022
Last Update Posted:
Feb 18, 2022
Last Verified:
Dec 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: