- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02963012
The Correlation Between Uterine Endometrial Pattern and Ectopic Pregnancy
November 14, 2016 updated by: Etty Spiegel, HaEmek Medical Center, Israel
A prospective trail. Pregnant women in the first trimester with positive BHCG and no visualization of gestational sac will be recruited.
The correlation between endometrial pattern and ectopic pregnancy will be assessed.
Study Overview
Study Type
Observational
Enrollment (Anticipated)
242
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
18 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Non-Probability Sample
Study Population
Women with ectopic pregnancy, in the first trimester.
Description
Inclusion Criteria:
- First trimester of pregnancy
- No visualization of gestational sac
Exclusion Criteria:
- Hemodynamic instability
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
- Observational Models: Case-Only
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
the corellation between presence and width of trilaminar endometrium as evaluated by transvaginal ultrasound and the diagnosis of ectopic pregnancy
Time Frame: first trimester of pregnancy
|
first trimester of pregnancy
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
December 1, 2016
Primary Completion (Anticipated)
December 1, 2019
Study Completion (Anticipated)
December 1, 2019
Study Registration Dates
First Submitted
September 12, 2016
First Submitted That Met QC Criteria
November 14, 2016
First Posted (Estimate)
November 15, 2016
Study Record Updates
Last Update Posted (Estimate)
November 15, 2016
Last Update Submitted That Met QC Criteria
November 14, 2016
Last Verified
November 1, 2016
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- emc 0164-15
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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