- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02765984
Relation of Implantation Site to Placental Site
March 6, 2018 updated by: Ahmed Maged, Cairo University
Relation of Implantation Site to Placental Site With or Without Cesarean Section Scar
Trans vaginal ultrasound with a partially full bladder will be done at gestational age earlier than 10 weeks to assess the site of intrauterine gestational sac to the endometrial cavity and the distance between the implantation site and the internal cervical os .
Doppler assessment of the retrochorionic blood flow at the area behind the maximum chorionic tissue to detect resistance index.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt, 12151
- Recruiting
- Ahmed Maged
-
Contact:
- Ahmed Maged, MD
- Email: prof.ahmedmaged@gmail.com
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-
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
20 years to 40 years (ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
pregnant women at their early trimester with or without cesarean section scar
Description
Inclusion Criteria:
- Single intrauterine pregnancy
- Gestational age less than 10 weeks
Exclusion Criteria:
- Any condition distorting uterine cavity as myoma, uterine anomalies.
- Absent fetal pulsations
- Any condition needing termination of early pregnancy as molar pregnancy or severe deteriorating maternal disease
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 |
|---|---|
|
normal placental site
women with normal implantation site at early trimester with normal placental site
|
transvaginal ultrasound done before 10 weeks gestational age measuring the distance between the lower end of the hyperechoic trophoblast ring of the gestational sac and the inner cervical os
|
|
Low placental site
women with low implantation site at early trimester with low placental site
|
transvaginal ultrasound done before 10 weeks gestational age measuring the distance between the lower end of the hyperechoic trophoblast ring of the gestational sac and the inner cervical os
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Distance between the implantation site and the internal cervical os
Time Frame: 10 weeks to 40 weeks gestational age
|
10 weeks to 40 weeks gestational age
|
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)
May 1, 2017
Primary Completion (ANTICIPATED)
December 1, 2018
Study Completion (ANTICIPATED)
December 1, 2018
Study Registration Dates
First Submitted
April 30, 2016
First Submitted That Met QC Criteria
May 5, 2016
First Posted (ESTIMATE)
May 9, 2016
Study Record Updates
Last Update Posted (ACTUAL)
March 7, 2018
Last Update Submitted That Met QC Criteria
March 6, 2018
Last Verified
March 1, 2018
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 142
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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