- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05228509
Portal Vein Flow Velocity as a Screening Tool for Oesophageal Varices in Cirrhotic Patients (Portalflow)
Study Overview
Status
Conditions
Detailed Description
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Peter At Rizk
- Phone Number: 01553529181
- Email: Peteratef662@gmail.com
Study Contact Backup
- Name: Atef Mu Rizk
- Phone Number: 01003938077
- Email: Peteratef669@gmail.com
Study Locations
-
-
Manfalout
-
Assiut, Manfalout, Egypt, 088
- Recruiting
- 43
-
Assiut, Manfalout, Egypt, 088
- Recruiting
- Egypt .assiut.manfalout
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- cirrhotic patients with oesophageal varices
- cirrhotic patients without oesophageal varices
Exclusion Criteria:
- Patients with hepato-cellular carcinomas [HCCs], portal vein thrombosis, hepatic encephalopathy.
- Patients with positive HCV antibody, but without liver cirrhosis diagnostic criteria
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Crossover
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Using upper GIT endoscopy to detect the presence or absence of oesophageal varices
Time Frame: 3 years
|
Non-invasive screening tool for esophageal varices: Aspartate aminotransferase-to-platelet ratio index (APRI) ... Doppler ultrasound of portal system Elastography both of liver and spleen... -Research outcome measures: a. Primary (main): Using upper GIT endoscopy to detect the presence or absence of oesophageal varices, and to detect the best and most available non- invasive predictor for it. |
3 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Peter At Munir, Master, Assiut University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Patef
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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