- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03205748
Evaluation of Different Etiologies of Obscure Ascites
November 28, 2017 updated by: Ahmed Mohamed Abbas, Assiut University
Evaluation of Different Etiologies of Obscure Ascites: Clinical, Laboratory, and Laparoscopic Study.
Ascites refers to fluid that accumulates within the peritoneal cavity.
Although ascites is most commonly observed in patients with cirrhosis and resulting portal hypertension (approximately 85% of cases), 7% to 10% of patients with ascites develop secondary to a malignancy
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
50
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
-
-
-
Assiut, Egypt
- Recruiting
- Assiut Faculty of Medicine
-
-
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
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All patients will be recruited from Departments of Internal Medicine, Assiut university tertiary hospital.
Description
Inclusion Criteria:
- Patients with ascites
- serum ascites albumin gradient >1.1.
Exclusion Criteria:
- ascitic fluid serum ascites albumin gradient <1.1.
- Haemorrgaic ascites;
- chylous ascites
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 |
Measure Description |
Time Frame |
---|---|---|
The percentage of patients with malignant ascites
Time Frame: 1 month
|
according to laboratory and clinical criteria
|
1 month
|
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)
August 1, 2017
Primary Completion (ANTICIPATED)
August 1, 2018
Study Completion (ANTICIPATED)
November 1, 2018
Study Registration Dates
First Submitted
June 29, 2017
First Submitted That Met QC Criteria
June 29, 2017
First Posted (ACTUAL)
July 2, 2017
Study Record Updates
Last Update Posted (ACTUAL)
November 29, 2017
Last Update Submitted That Met QC Criteria
November 28, 2017
Last Verified
November 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- OA
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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