- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06083727
Primary Cesarean Section in Primigravida and Muligravida in Sohag and Al Balyana Cities
October 9, 2023 updated by: Sahar Nasser Fathy, Sohag University
cesarean section and vaginal delivery are two methods of delivery, cesarean section somtimes indicated for obstetrical reason but primary cesarean section especially in primigravida might have a preference of the mode of delivery
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
100
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
- Name: Sahar N Fathy, resident
- Phone Number: 01146577899
- Email: sahernasser@med.sohag.com
Study Contact Backup
- Name: Salah M Rasheed, professor
- Phone Number: 01224653702
Study Locations
-
-
-
Sohag, Egypt, sohag
- Recruiting
- Sohag University
-
Contact:
- Magdy M Amin, Professor
- Email: portal@med.sohag.edu.eg
-
-
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
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
all primigravida with gestational age more than 28 weeks and above who have come for delivery
- multigravida upto gravida 4 with gestational age more than 28 weeks and above who has had one previous viable vaginal delivery
- women between 18 and 45 years
Description
Inclusion Criteria:
- all primigravida with gestational age more than 28 weeks and above who have come for delivery
- multigravida upto gravida 4 with gestational age more than 28 weeks and above who has had one previous viable vaginal delivery
- women between 18 and 45 years
Exclusion Criteria:
- primigravida women <28 weeks
- multigravida <28 weeks
- patient having previous history of myomectomy or hystrotomy
- gravida 5 and more
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 |
|---|---|
|
primigravida
|
rate of primary cesarean section in primigravida and multigravida
|
|
multigravida
|
rate of primary cesarean section in primigravida and multigravida
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
rate
Time Frame: 6 months
|
rate of primary cesarean section
|
6 months
|
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 (Actual)
September 24, 2023
Primary Completion (Estimated)
March 24, 2024
Study Completion (Estimated)
March 24, 2024
Study Registration Dates
First Submitted
October 9, 2023
First Submitted That Met QC Criteria
October 9, 2023
First Posted (Actual)
October 16, 2023
Study Record Updates
Last Update Posted (Actual)
October 16, 2023
Last Update Submitted That Met QC Criteria
October 9, 2023
Last Verified
October 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- Soh-Med-23-09-03MS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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