Effect of Natural Cesarean Section on Breastfeeding
June 19, 2015 updated by: Samer mohamed ahmed, Ain Shams University
Effect of Natural Cesarean Section in Comparison to Traditional Cesarean Section on Maternal and Fetal Recovery
Effect of natural cesarean section in comparison to traditional cesarean section on maternal and fetal recovery.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
100
Phase
- Not Applicable
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
16 years to 36 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- primigravida or para one section
- full term
- cephalic
- single baby
- average weight
- spinal anathesia
Exclusion Criteria:
- High risk pregnancy.
- Women with known or suspected fetal malformation.
- Women with uterine malformations.
- Breech or transverse lie.
- Emergency caesarean section.
- Previous two or more caesarean section
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
- Primary Purpose: Screening
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: group A
natural cesarean section
|
|
|
Other: group B
traditional cesarean section
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
time to start breastfeeding
Time Frame: 3 hrs
|
3 hrs
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
June 1, 2015
Primary Completion (Anticipated)
February 1, 2016
Study Completion (Anticipated)
February 1, 2016
Study Registration Dates
First Submitted
June 13, 2015
First Submitted That Met QC Criteria
June 19, 2015
First Posted (Estimate)
June 24, 2015
Study Record Updates
Last Update Posted (Estimate)
June 24, 2015
Last Update Submitted That Met QC Criteria
June 19, 2015
Last Verified
June 1, 2015
More Information
Terms related to this study
Other Study ID Numbers
- Nsc_123
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.