- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03471780
Evaluation of Transperineal US in Labour
January 8, 2019 updated by: Mahmoud Alalfy, Aljazeera Hospital
The Importance of Transperineal US in Labour
Assessment of progress of labour is an important step in decision making of obstetricians
Study Overview
Detailed Description
delayed progress of labour resemble an annoying problem to obstetrician so noninvasive diagnostic methods can play an important role in implementing a guidelines to follow patients in labour as transperineal US .
Study Type
Observational
Enrollment (Anticipated)
600
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
-
-
-
Giza, Egypt
- Recruiting
- Algazeerah
-
-
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 40 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
- pregnant women in labour
- Full term
Description
Inclusion Criteria:
- pregnant women in labour
- Full term
Exclusion Criteria:
- pregnant ladies not in labour
- Preterm labour
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
the number of participants who will deliver by normal delivery
Time Frame: within 24 hours
|
within 24 hours
|
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 (Actual)
January 8, 2018
Primary Completion (Anticipated)
April 10, 2019
Study Completion (Anticipated)
April 10, 2019
Study Registration Dates
First Submitted
March 14, 2018
First Submitted That Met QC Criteria
March 14, 2018
First Posted (Actual)
March 21, 2018
Study Record Updates
Last Update Posted (Actual)
January 9, 2019
Last Update Submitted That Met QC Criteria
January 8, 2019
Last Verified
January 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- labour US
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
IPD Plan Description
no plan is decided now
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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