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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03172013
Other study ID # eldemerdash
Secondary ID
Status Recruiting
Phase N/A
First received May 27, 2017
Last updated May 30, 2017
Start date May 11, 2017
Est. completion date December 2019

Study information

Verified date May 2017
Source Tanta University
Contact Sherief Abd-Elsalam, consultant
Phone 00201095159522
Email Sheriefabdelsalam@yahoo.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Spontaneous bacterial peritonitis (SBP) is an ascitic fluid infection in cirrhotic patients


Description:

Platelet indices can be utilized as a non-invasive predictor of SBP.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Cirrhotic patients and ascites

Exclusion Criteria:

- patients with ascites due to causes other than cirrhosis- immunocompromised patients,

- patients with abnormal thrombocytes due to non-hepatic causes.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Platelet indices
MPV, PDW

Locations

Country Name City State
Egypt Tanta university hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Tanta University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of patients with SBP and abnormal platelet indices Number of patients with SBP and abnormal platelet indices 6 months
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