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Early Versus Traditional Oral Hydration After Cesarean Section

Early Versus Traditional Oral Hydration After Cesarean Section; A Randomized Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03442634
Enrollment
2
Registered
2018-02-22
Start date
2018-03-01
Completion date
2018-06-30
Last updated
2018-08-09

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

Conditions

Gastrointestinal Motility and Defecation Conditions

Keywords

bowel movements, cesarean section, oral hydration

Brief summary

this study helps us to compare and evaluate prospectively the benefits and safety of early hydration on bowel movement after cesarean section it includes two groups, a control group and a study group. the study group will get 200 ml of sugar free water within 1 hour after cs while the control group will get 200 ml of sugar free water 6 hours after cs

Detailed description

Traditionally, patients are not given fluids or food after cesarean sections until bowel function returns as evidenced by bowel sounds, passage of stool or flatus since , uneventful (uncomplicated) cesarean sections have no effect on intestinal functions and with putting in minds the need of the mother for early hydration , movement , breast feeding and early discharge; that is why we are investigating the effectiveness and safety of early oral hydration after cesarean sections

Interventions

this group will start oral hydration within 1 hour after cesarean section

OTHERTraditional Oral Hydration

this group will start oral hydration 6 hours after cesarean section

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
Yes

Inclusion criteria

* Term Singleton Pregnancy. * Uncomplicated Elective Cesarean Section. * Time of Cesarean Section doesn't exceed 90 minutes. * Average blood loss during and after cesarean section (doesn't exceed 1000cc). * All patients will be under spinal anesthesia.

Exclusion criteria

* Postpartum Hemorrhage. * Surgical Complications Such as intestinal injury. * Medical disorders such as Diabetes and Hypertension * Factors that may influence postpartum blood loss as anemia, multiple pregnancy and polyhydraminos. * Use of tocolytic drugs

Design outcomes

Primary

MeasureTime frameDescription
audible intestinal soundsfirst 12 hours after cesarean sectionauscultation of intestinal sounds hourly for the first 12 hours after cesarean section

Secondary

MeasureTime frameDescription
time for first breast feedingfirst 24 hours after cesarean sectionrecording the time of first breast-feed
abdominal distensionfirst 24 hours after cesarean sectionrecording the incidence of abdominal distension after cesarean section
amount of given intravenous fluidsup to 24 hours after cesarean sectionrecording amount in ml of given iv fluids
need for pain analgesicsup to 24 hours after cesarean sectionrecording the amount of pain analgesia needed after cesarean section
postoperative anorexia, nausea and vomitingfirst 24 hours after cesarean sectionrecording the incidence of git upset symptoms in the first 24 hours after cesarean section
satisfaction measured with a visual analogue scale before patient dischargefirst 6 hours after cesarean sectionmeasuring satisfaction level after cesarean section
time to first flatusup to 48 hours after cesarean sectionrecording the time at which the patient had its first flatus
time to first bowel movementup to 72 hours after cesarean sectionrecording the time at which the patient had her first bowel motion
length of hospital stayup to 48 hours after cesarean sectionrecording the length of patients' stay at hospital

Countries

Egypt

Outcome results

None listed

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