Early Versus Traditional Oral Hydration After Cesarean Section

NCT ID: NCT03442634

Last Updated: 2018-08-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-01

Study Completion Date

2018-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Gastrointestinal Motility and Defecation Conditions

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Early Hydration Group

this study group will get 200 ml of sugar free water within 1 hour after cesarean section followed by oral hydration as per patients' desire then starting semisolid and solid foods when patients are open bowel Intervention: Early Oral Hydration

Group Type EXPERIMENTAL

Early Hydration

Intervention Type OTHER

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

Traditional Hydration Group

this study group will get 200 ml of sugar free water after 6 hours after cesarean section followed by oral hydration as per patients' desire then starting semisolid and solid foods when patients are open bowel Intervention: Traditional Oral Hydration

Group Type ACTIVE_COMPARATOR

Traditional Oral Hydration

Intervention Type OTHER

this group will start oral hydration 6 hours after cesarean section

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Early Hydration

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

Intervention Type OTHER

Traditional Oral Hydration

this group will start oral hydration 6 hours after cesarean section

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Early Oral Hydration Delayed Oral Hydration

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

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
Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Ain Shams University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Mohamed Hassan Mohamed Mostafa

Obstetrics and Gynaecology Resident

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Bassem A Islam, Lecturer

Role: STUDY_DIRECTOR

Ain Shams Maternity Hospital

Karim A Wahba, Professor

Role: STUDY_DIRECTOR

Ain Shams Maternity Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ain Shams Maternity Hospital

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

cshydration

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.